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HPKM 88691 have HNPCC/Lynch syndrome usually have an MSS/MSI-L phenotype (MSI at 90% of mutations detected in the cationic trypsinogen gene, the inability to identify mutations in approximately 20% of families with HP suggests the possible Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or MayoMedicalLaboratories.com Page 919
HP 83019 HSEP 81087 involvement of other loci or unidentified mutations in the cationic trypsinogen gene. Useful For: Confirming the diagnosis of hereditary pancreatitis in patients with chronic pancreatitis who also have a family member with a documented PRSS1 gene mutation Screening of at-risk individuals when a mutation has been identified in an affected family member Interpretation: An interpretive report will be provided. Reference Values: An interpretive report will be provided. Clinical References: 1. Teich N, Mossner J: Hereditary chronic pancreatitis. Best Pract Res Clin Gastroenterol. 2008;22(1):115-30 2. Howes N, Greenhalf W, Stocken DD, Neoptolemos JP: Cationic trypsinogen mutations and pancreatitis. Clin Lab Med 2005;25:39-59 3. Ellis I: Genetic counseling for hereditary pancreatitis--the role of molecular genetics testing for the cationic trypsinogen gene, cystic fibrosis and serine protease inhibitor Kazal type 1. Gastroenterol Clin North Am 2004;33:839-854 Hereditary Pancreatitis, Mutation Screen Clinical Information: Hereditary pancreatitis (HP) is a rare autosomal dominant disorder, with approximately 80% penetrance. HP is characterized by early onset of acute pancreatitis during childhood or early adolescence. The acute pancreatitis in these patients generally progresses to chronic pancreatitis by adulthood and can eventually lead to both exocrine and endocrine pancreatic insufficiency. Patients with HP are also at an increased risk for developing pancreatic cancer. Studies have estimated the lifetime risk of developing pancreatic cancer to be as high as 40%. HP cannot be clinically distinguished from other forms of pancreatitis. However, PRSS1 mutations are generally restricted to individuals with a family history of pancreatitis. PRSS1 mutations are infrequently found in patients with alcohol-induced and tropical pancreatitis. The protease serine 1 or cationic trypsinogen (PRSS1) gene is located on chromosome 7. It has been reported that as many as 80% of patients with symptomatic hereditary pancreatitis have a causative PRSS1 mutation. Although several mutations have been identified, the Arg122His (R122H), Asn29Ile (N29I), and Ala16Val (A16V) mutations have been identified as the primary causative defects in HP. The phenotype of patients with these 3 mutations is quite similar, sharing many clinical features, though there are some differences. Data suggests that the R122H mutation results in more severe disease and earlier onset of symptoms, while the A16V mutation has reduced penetrance. Although these 3 alterations account for >90% of mutations detected in the cationic trypsinogen gene, the inability to identify mutations in approximately 20% of families with HP suggests the possible involvement of other loci or unidentified mutations in the cationic trypsinogen gene. Useful For: Confirming the diagnosis of hereditary pancreatitis (HP) in patients with chronic pancreatitis Ruling out HP in patients with chronic pancreatitis Interpretation: An interpretive report will be provided. Reference Values: An interpretive report will be provided. Clinical References: 1. Teich N, Mossner J: Hereditary chronic pancreatitis. Best Pract Res Clin Gastroenterol 2008;22(1):115-30 2. Howes N, Greenhalf W, Stocken DD, Neoptolemos JP: Cationic trypsinogen mutations and pancreatitis. Clin Lab Med 2005;25:39-59 3. Ellis I: Genetic counseling for hereditary pancreatitis-the role of molecular genetics testing for the cationic trypsinogen gene, cystic fibrosis and serine protease inhibitor Kazal type 1. Gastroenterol Clin North Am 2004;33:839-854 Hereditary Spherocytosis Evaluation Clinical Information: The hemolytic anemias are a group of anemias that are characterized by an increased destruction of RBCs. Anemias may be divided into inherited or acquired. Hereditary spherocytosis (HS), also known as congenital hemolytic anemia, is inherited as a non sex-linked dominant trait. HS is caused by a RBC membrane defect. The RBCs are spherocytic in shape and show an increased Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or MayoMedicalLaboratories.com Page 920
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Rochester 2013 Interpretive Handboo
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Policies - Mayo Medical Laboratorie
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TTIG 82506 DHVD 8822 Tetanus Toxoid
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DCRN 8847 Identification of patient
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DOC 8547 function primarily, 18-hyd
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FDSOX 91690 THCM 84284 11-Desoxycor
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FBP1 86208 Normal: or =1.5 ng/mL;
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17OHP 81151 Pediatric Reference Ran
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OHPG 9231 2000;52(5):601-607 4. Kao
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FP73 88541 Interpretation: The pres
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OH21 81970 21-deoxycortisol may be
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CYPKP 89082 transcriptionally activ
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25HDN 83670 25-Hydroxyvitamin D2 an
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F5HAR 57333 HIAA 9248 can also be a
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6MAMU 89605 converts heroin into 6-
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ACAC 82757 ACANT 80401 increase the
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ACM 8698 FACTO 90247 1 0.35-0.69 Eq
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ACHS 8522 Clinical Information: Neu
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ACT 8221 APT 9058 and isolation of
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AHPS 9022 ancestry. Homozygosity fo
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FAML secretions, but it is not comm
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ACRN 82413 Acylcarnitines, Quantita
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or =8 years:
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ADM13 61212 studies (enzyme assay,
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FADA 91554 81444 (50-70 x normal) A
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FADE 91670 LADV 89074 LCADP 89887 A
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FADMK 91925 RACTH 82140 ADmark Phos
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AGXMS 89915 7 year 2-88 8 year 5-71
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the third decade of life, but can o
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FALUF 57286 ALB 8436 involved in th
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FALCO 90084 ALS 8363 ALDNA 15150 th
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ALDU 8556 regulator of the synthesi
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ALKI 89503 11 years: 185-507 U/L 12
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17-23 years: 52-144 U/L 24-45 years
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FALMD 92001 ALM 82882 Almond (Amygd
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FASU 91221 FA1AG 90464 19-70+ years
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A1APP 26953 genotype is at greater
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A1M24 81036 RA1M 84448 605-608 2. M
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A2M 9270 AAMY 82866 Alpha-2-Macrogl
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AFP 8162 hepatocellular carcinoma,
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AFPSF 8876 Screen [Second Trimester
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FUCW 8814 molecules in the tissues
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AGA 8785 disease. In female patient
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AGPB 9499 IDSWB 60618 disease. In T
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IDST 8780 categorized into 3 syndro
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MANT 8773 MANN 8772 5 50.0-99.9 Str
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ANAS 8782 APGH 9003 Alpha-N-Acetylg
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ALPA 500155 Tanner II-IV*: < or =1.
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ALUR 86377 -Aluminum-laden albumin
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86375 exposure. This was done by sw
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FAMAN 91132 AMKPK 82112 possible ev
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AAMSD 60200 susceptible strains of
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Serine (Ser) 69-271 71-208 63-187 H
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Glutamine Gln 139-2985 263 -2979 15
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AAUCD 60202 Glutamic Acid (Glu) 1-M
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FALAU 57350 ALADW to secondary inhi
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AMIO 9247 dehydratase (ALAD) activi
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AMOBS 8325 FAMOX 80450 FMAXN 57245
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AMPCC 61514 receptors that mediate
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FAMPH 90113 AMPHU 8257 MJ, Parks PM
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AMBF 8371 immune response to allerg
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PAMYB 5079 PAMY 80376 Clinical Refe
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AMSU 8356 AMS 8352 Amylase, Timed C
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AMYL 83667 AMYKM 83705 provided. Re
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ANAP 81157 TTR-associated familial
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F3AAG 57109 ANST 9709 Class IgE kU/
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FPOC 81081 correlate only modestly
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FANGI 90429 FANG 90428 Interpretati
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FANSD 91955 FAEAB 91854 immunoglobu
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FANBF 57173 FCLNE 91321 FPHET 91322
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ABTIH 9000 ENAE 89035 Antibody Tite
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MMLYP 81602 MMLRG 81601 Test Perfor
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MMLSA 56031 MACCL 89218 antimicrobi
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FAMS 91540 Clinical Information: No
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VASC 83012 evaluation for infertili
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ANA2 9026 ATTF 9030 Antinuclear Ant
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ATTI 9031 Antithrombin Antigen, Pla
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APO1K 60724 APO2S 60725 Shiller SM,
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APLAB 80318 APLA1 80309 mutation in
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APOE 80905 expressing more severe d
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APR 82835 AWNS 87814 6 > or =100 St
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ARBOP 83267 Reference values apply
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distinguishable from comparison gro
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FARI 57112 FARIX 57123 FCGHP 89858
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ARSAS 61259 ARSAK number variation
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ASFRU 84679 forms. Concentrations >
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ASHA 8651 and their partially detox
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ASCRU 89890 are nontoxic, inorganic
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ARSAW 8779 Useful For: Detection of
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ARSB 8151 ASCRI 82764 Roth. McGraw-
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AJPWO 88887 Clinical References: 1.
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AST 8360 clinical manifestations. I
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FASP 91607 ASPBA 61009 antigen in f
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SASP 9678 ASPG 86324 Aspergillus fu
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FAPP 91428 Reference Values: or =1
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APIN 82803 responsible for elicitin
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AGIDE 89886 < or =0.02 nmol/L NEURO
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ALDE 84248 anti-neuronal nuclear au
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FAVI 91509 AVOC 82812 approximately
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CD40 89009 conventional cytogenetic
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80027 IABCS 88800 patients with B-c
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B-cell-depleting immunotherapy Iden
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functional classification system fo
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FBAB 91608 BABG 81128 5785 Corporat
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GEN 8108 SPUT 8095 Bruyn G, Pieniaz
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CFRC 89653 EPRP 60235 result in int
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BAHG 82711 BCYP 82722 electrophores
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BANA 82746 sensitization to particu
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BRLY 82687 caused by the release of
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FBART 91439 BART 81575 amplificatio
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BARTB 89983 BASL 82489 B. bacillifo
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BADX 89006 Interpretation: Detectio
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MBCR 80578 helpful for both prognos
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FBBCK 91664 FBEAN 91646 ASPE/Lumine
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BECH 82669 of IC2 (LIT1) is hypothe
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BEEF 82697 BEETS 82618 Beef, IgE Cl
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FPHEN 91136 FBEN 90294 BENZU 80370
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BBEET 82838 BERG 82892 Berlin Beetl
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AB2GP 86180 Negative (reported as p
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GB2GP 86182 or =15.0 U/mL (positiv
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BETA2 80351 patients with APS.(4) A
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B2MU 300243 B2M 9234 Livanainen M,
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BGAW 60987 Postmenopausal: 104-1,00
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BGAT 8008 beta-galactosidase defici
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BGLT 8787 BGL 8788 B disease. Clini
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BHCG 61718 Sly syndrome is 1 of the
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BLACT 8118 BLAC Clinical Informatio
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and the determination of bicarbonat
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84357 19701 Interpretation: Total b
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BFBL 34621 the color of bilirubin a
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BILIT 81785 Bilirubin, Total, Serum
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BIOTS 88205 levels of biotinidase,
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FBISU 91142 LCBK 88910 Test Perform
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QBKU 87859 Useful For: As a prospec
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SBLAS 86691 antibodies interact wit
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80326 BDIAL 83094 night sweats. It
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UEBF 81834 BWOR 82840 urinary tract
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BLUE 82359 Clinical Information: Cl
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BHINT 9027 resorption is balanced b
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BPRP 80910 FBPTS 57290 An interpret
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BOAC 9723 BOT 82715 Cypress, CA 906
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89045 proteins) followed by respira
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BRAZ 82899 MLH1 promoter hypermethy
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BMNA 81976 FYSTB 91990 BROC 82817 C
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BRM 8608 BRUGM 89476 0 Negative 1 0
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BRUTA 8112 brucellosis may include
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manifests in male children younger
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clinical phenotype can vary conside
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BTKK 89306 Useful For: Confirming a
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BUCW 82727 XLA patients are diagnos
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BFTH 82779 identify allergens which
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BUPIS 89548 BUPM 500038 membrane pr
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FBUS 91115 BUAUC 83188 increase in
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FCPEP 91270 anti-insulin autoantibo
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C1ES 8198 Useful For: Assessment of
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C1QFX 83374 Reference Values: C1Q B
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C2 81835 receptors. The absence of
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FC3D 91725 C4U 88829 C4FX 83391 C3d
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C5FX 83392 C5DCU 88831 1987;76:939-
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C7FX 81064 complement system is com
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C9FX 81066 CABB 86327 4. Gaither TA
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CDOMB 89539 CDOM 80595 Reference Va
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CDRU 60156 CAFF 8754 years) is the
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3 10.7-15.4 17-72 4 11.8-16.2 15-11
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FCAH1 91275 1 - 7m: Levels decrease
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Males: Levels increase after the fi
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Units: ug/dL Age Range Premature (2
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4 10.7-15.6 47-208 5 11.8-18.6 50-2
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anging from 40 - 200 between 30 and
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Clinical Information: In the normal
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CSRMS 83703 hypoparathyroidism, a s
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CAU 8594 CAF 8379 An interpretive r
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CAUR 60157 CAS parathyroid hormone-
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CACRU 89604 important role in blood
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CAVPC 83900 excretion of calcium is
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FCALP 91597 FCAMP 91224 CFTH 82778
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CANW 81780 CA25 9289 1 0.35-0.69 Eq
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FCANA 57158 testing often depend up
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FFTH 90479 FCAPR 90062 CWAY 82493 C
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CAR 8654 C1011 80682 total and free
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199PC 89508 199PT 61530 Clinical Re
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CA19 9288 CDG 89891 Carbohydrate An
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CHOU 9255 COHBB 8649 isoforms (ie,
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CEAPT 61528 PFCEA 83742 Carcinoembr
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CEASF 8918 CARD 82491 Carcinoembryo
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CPTKM 61121 CARN 8802 screening can
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cycle, or secondary disturbances in
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CACTK 61195 CAROB 82368 analysis. U
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FCASE 91647 caused by the release o
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FCASO 91995 CBN 82770 sensitivity t
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COMTO 60336 1 0.35-0.69 Equivocal 2
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CATU 9276 An interpretive report wi
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neuropathies are characterized by e
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CBC 9109 Useful For: Testing for Ig
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15 days-1 month: 31.0-55.0% 2-5 mon
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CD20B 89584 CD20 on B Cells Clinica
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3-5 months: 51-77%* 6-11 months: 49
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55 years: 49-87% % Helper cells (CD
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GLICP 89369 essential to serially m
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T- AND B-CELL QUANTITATION BY FLOW
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GLIC 89317 H/S ratio: > or =1.0 *Sh
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a more recent thymic ontogeny where
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CDKKM 60229 Med Genet 1999;36:518-5
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CELY 82766 CDCOM 89201 Company, 200
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CDGF 89200 serology does not exclud
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CELI 88906 range. For these individ
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5368 CMA 9278 autoantibodies can be
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CTSA 81979 sensitization to particu
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CERE 8364 patients with multiple sc
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8032 80199 2002 April ;287(16):2114
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CFTRK 88880 deferens or pancreatiti
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CCHZ 82752 MCHZ 82751 Test Performe
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CTRE 82607 likelihood of allergic d
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CHXP 82494 Clinical Information: Im
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CHCK 82713 CSPR 82351 5 50.0-99.9 S
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CHILI 82499 and to define the aller
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CHRGB 83186 CHPA 80411 FCPP 57339 S
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CGRNA 61553 Clinical References: 1.
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FCTRC 91659 CDFAW 110502 are requir
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FCPC 90439 FCPD 91750 FCHH 90111 pr
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CLFT 60028 CLBF 8470 CLF 8467 as hi
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CLSF 8218 CLU 8531 FCCK 90162 > or
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HDCH 8429 CHOL 8320 Serous Body Flu
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BHSF 8877 FCHAB 91900 serum may inc
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CR 86153 concentrations in the abse
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(5-hydroxytryptamine: 5-HT) and pep
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POC 8887 CVS 80257 An interpretativ
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CMS 8696 HBL 8537 deletions in 13q1
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LN 8911 SCE 926 Chromosome Analysis
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SBK 89338 to summarize here. The re
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CHSBP 9023 process. A normal karyot
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FCLL 83089 Negative Interpretation
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CHYM 82609 the urine (chyluria) is
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CTCB 89089 CTCC 89162 This test was
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RCITR 84773 CITR 9329 Reference Val
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CLAM 82884 proteins) followed by re
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CLLM 60490 Reference Values: An int
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CLOS 80424 CDRP 83124 Sedation has
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FCMVQ 91734 recurrent suicidal beha
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F_9 9065 FACTV 9054 Adults: 75-145%
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F7IS 7809 F8A 9070 prolonged prothr
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FXCH 89042 F10IS 7811 Coagulation F
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F_12 9069 COU 80083 Basic Principle
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COS 80084 COBCU 60353 Cobalt, Serum
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COKEU 9286 fluid.(7) The first evid
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CCOC 81542 Interpretation: Compleme
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COCR 82693 clinical manifestations.
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COD 82889 Q10 87853 5 50.0-99.9 Str
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CAGG 8992 FFTYC 91496 CTF 80440 Col
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CVID 87993 testing often depend upo
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C4 8171 AH50 88676 Clinical Informa
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FCCEV 57461 FFDMC 91581 FMDMC 91578
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CAH21 87815 congenital adrenal hype
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CTDC 83631 Reference Values: An int
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CURU Interpretation: The constellat
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CUCRU 60427 CORI can cause hypocupr
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CRNP 82718 CORN 82705 Corn Pollen,
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sex steroids. Synthesis proceeds fr
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FCBG 90148 FCORT 91644 CRANU 82920
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CORTU 8546 Cortisol, Serum (ug/dL)
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CORT 8545 measurements, midnight bl
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COCRU 88903 serum and urine cortiso
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hydrocortisone) increases and is fi
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CSED 82804 Class IgE kU/L Interpret
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FACX 91340 immune response to aller
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89366 CPOXS 61263 CPM, 12q15, for W
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CRANB 86307 bronchospasm) in infant
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CRDPU 88697 6 > or =100 Strongly po
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CKMB 82429 CK 8336 Creatine Kinase
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CREAZ 8472 13-36 months: 0.1-0.4 mg
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CRBF 8037 RCTUR 83802 guidelines fo
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CRGSP 83659 CRY_S 80988 Clinical Re
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CCRYP 86166 CRYPF 60320 in serum sp
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CRYPU 60319 Clinical Information: C
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CUKE 82861 Reference Values: Anti-T
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WHTC 82915 proteins) followed by re
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VRID2 5190 FCMSD 92004 CURR 82498 C
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60506 CIFS 8052 Cutaneous Anaplasti
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CYAN 8691 GRP 8771 pattern at the B
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CYCL 81506 CYCSP 8931 Reference Ran
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insufficiency. The incidence of CF
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CYSR 81067 distinguished by the pat
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drugs and environmental factors. Us
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2C19S 60439 activity include: -Broc
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including the intestines and liver.
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2C9SO 60337 Interpretation: An inte
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2613delAGA Decreased activity *10 1
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2D6TO 60340 an interpretation indic
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antidepressants, antiemetics, antih
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3A4O 61242 individual is homozygous
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CMG 80750 known. A ratio of > or =2
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e seen after acute illness, immunos
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and have cytotoxic function in resp
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ANCA 9441 Clinical Information: Cyt
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DLAC 8878 DLAU 8873 fibrinogen equi
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DAND 82694 FDANT 90363 5 50.0-99.9
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DATRE 82481 9803 DEEP 82144 Date, T
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observed at birth. Levels then decl
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diagnostic accuracy than DHEA-S mea
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FDOC 90134 5468 children. Character
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DESIP 81854 DSG13 83680 1 0.35-0.69
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FDXM 91956 FDEXA 91777 diagnosis, t
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DIA 8629 FDIGS 91454 Clinical Refer
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DIG 8674 FDPD 57141 American Associ
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DILL 82602 serum levels. Patients w
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DIP 83262 DTAB 83269 FDIPY 90371 Co
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FDISP 91595 DSP 8220 Sucrase: Range
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FDKYL 91960 DOGD 60108 Increases of
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DRD3O 60342 should be monitored clo
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DRD4O 60344 Reference Values: An in
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FDOXY 90061 CDAU1 80917 doxepin and
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CDAU3 80919 spectrometry (GC-MS) th
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IDOAU 8248 (GC-FID) the following d
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DABAR 505335 Urine Clinical Informa
Page 637 and 638:
DMETH 505343 DPCP 505339 EMIT cutof
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DTHC 505331 and kidney. Toxic manif
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DSS 8421 CDAS 500752 Drugs of toxic
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FBDAS 91776 FMP10 57505 FBD 57117 D
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DASM4 60553 spectrometry (LC-MS/MS)
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DULOX 89305 immunoglobulin E (IgE)-
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ESYC 82721 infected individuals, it
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FECHC 91342 ECHO 80293 concentratio
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FEGFR 91903 FEGGW 91976 EGG 82872 W
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EGGP 82477 concentration of IgE ant
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FECHA 91710 EHRL 84319
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ELDR 82392 ELPN 87972 No pediatric
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EFP 81488 SODIUM 0-15 years: not es
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PEL 80085 chain fragments as well a
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ELM 82672 PROTEIN, TOTAL > or =18 y
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Reference Range: IgG
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5362 FEMA 91836 EMA 9360 anatomic p
Page 671 and 672:
SAM 9049 FEHA 91932 Interpretation:
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FENTQ 91312 LENT 80066 INTERPRETIVE
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FEPHD 90109 EPUR 82854 presence of
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SEBV 84421 Clinical Information: Cl
Page 679 and 680:
80786 EBVA 8891 antigen. The presen
Page 681 and 682:
LEBV 81239 EBVB 87439 with type 1 N
Page 683 and 684:
REVP 84160 M, Emre S, et al: Prospe
Page 685 and 686:
EPOR 61679 FESC 91458 FFES no eryth
Page 687 and 688:
primarily in ovaries and testes by
Page 689 and 690:
UE3 81711 Stage V 18 years 10-40 pg
Page 691 and 692:
ESTF 84230 Immunohistochemistry, Ma
Page 693 and 694:
preparations). The gonadotrophin-re
Page 695 and 696:
E1 81418 Stage V 14.5 years 15-350
Page 697 and 698:
are due to problems in androgen sig
Page 699 and 700:
ETOHU 500323 ETX 8769 Interpretatio
Page 701 and 702:
EOXD 82767 EUCL 82758 Ethylene Oxid
Page 703 and 704:
EHOR 82662 0 Negative 1 0.35-0.69 E
Page 705 and 706:
83363 fluorescence in situ hybridiz
Page 707 and 708:
F9INH 83103 lysosomes of both perip
Page 709 and 710:
F8INH 83102 FX13M 57302 FOGT Clinic
Page 711 and 712:
FAPKM 83001 and to define the aller
Page 713 and 714:
FD 85319 LDLRS 81013 features This
Page 715 and 716:
LDLM 89073 Useful For: Genetic test
Page 717 and 718:
FANCA 85318 FATF 8310 separately or
Page 719 and 720:
FAPCP 82042 Clinic or elsewhere, an
Page 721 and 722:
or =18 years: 30-450 nmol/mL Hexade
Page 723 and 724:
Hexacosanoic Acid, C26:0 0.00-1.30
Page 725 and 726:
1-17 years: 9-130 nmol/mL > or =18
Page 727 and 728:
FAPM 81939 or =18 years: 7.3-16.8
Page 729 and 730:
POX 81369 oxidation disorders. Ann
Page 731 and 732:
FBN1 89308 range of variability, in
Page 733 and 734:
FETH2 81880 FFAPL 57379 Delineation
Page 735 and 736:
FOBT 60693 Useful For: Suggesting p
Page 737 and 738:
FENTU 89655 testing often depend up
Page 739 and 740:
FERR 8689 Clinical Information: Cli
Page 741 and 742:
FECHK 60372 biochemical genetic tes
Page 743 and 744:
FMBNY 30320 pregnancy, as well as b
Page 745 and 746:
FGAKM 60722 in order to provide an
Page 747 and 748:
FIBR 8482 FBC 80333 FGF23 88662 Fem
Page 749 and 750:
FFIL4 90068 FIL 9232 The detected c
Page 751 and 752:
FANT 82698 FBSH 82735 Laboratory Me
Page 753 and 754:
9804 FLEC 9243 growth factor-bindin
Page 755 and 756:
FFLRO 91795 FL 8641 impaired patien
Page 757 and 758:
FFLUR 90091 17BFP 89739 ST. PAUL, M
Page 759 and 760:
FSH 8670 folate deficiency states.
Page 761 and 762:
FDP1 86207 antibodies interact with
Page 763 and 764:
FOOD4 81872 3 3.50-17.4 Positive 4
Page 765 and 766:
FOOD1 81868 sensitivity to inhalant
Page 767 and 768:
FOOD3 81871 FRMH 82869 Clinical Ref
Page 769 and 770:
9881 60694 Reporting limit determin
Page 771 and 772:
FRANC 91552 other FMR1-related diso
Page 773 and 774:
FFRED 91819 FFRBS 60476 Reference V
Page 775 and 776:
FRUCT 81610 FROS 81164 GFDMS protei
Page 777 and 778:
FSS 83121 FSC 83120 family member.
Page 779 and 780:
FGEN 84389 FVAG 5184 after 30 days
Page 781 and 782:
FFURO 91119 FUSM 82750 Furosemide (
Page 783 and 784:
GABA 80826 cerebrospinal fluid may
Page 785 and 786:
GDUR 89316 myocardium have also bee
Page 787 and 788:
GALK 8628 associated with the nephr
Page 789 and 790:
GALU 8765 GAL1P 80337 Galactose, Qu
Page 791 and 792:
GALTP 80341 of GALT enzyme activity
Page 793 and 794:
GALTK 84367 (galactose and galactos
Page 795 and 796:
CBGT 8297 frequently observed mutat
Page 797 and 798:
GCC 81981 Galectin-3 is a biomarker
Page 799 and 800:
GGT 8677 interpretation and reporti
Page 801 and 802:
GM1B 83189 Ganglioside Antibody Pan
Page 803 and 804:
FGIP 90171 GAST 8512 1 0.35-0.69 Eq
Page 805 and 806:
GBAMS 60711 GBAKM 60712 fasting per
Page 807 and 808:
GELA 86326 diagnosis in at-risk pre
Page 809 and 810:
GENPK 84695 GENT 81750 amyloidosis,
Page 811 and 812:
GERB 82545 89713 Am Fam Physician 1
Page 813 and 814:
GRAB 80628 GIAR 80231 3 3.50-17.4 P
Page 815 and 816:
DGLDN 89031 2 0.70-3.49 Positive 3
Page 817 and 818:
equires a jejunal biopsy demonstrat
Page 819 and 820:
FGLIP 91097 GBM 8106 Disease Diagno
Page 821 and 822:
GPI 9158 GLBF 8343 then rise again
Page 823 and 824:
RGLUR 89847 GLSF 152 GLUR 8412 Gluc
Page 825 and 826:
GD65C 84221 marker of predispositio
Page 827 and 828:
FGLYA 57287 FGLMA 91742 sensitizati
Page 829 and 830:
GMILK 82550 sensitivity to inhalant
Page 831 and 832:
9810 9812 FGNRH 90165 GOOS 82714 Cl
Page 833 and 834:
GRAM 8078 81990 LAGGT 8976 Referenc
Page 835 and 836:
GRFR 82836 GRAS1 81706 Laboratory M
Page 837 and 838:
GRAS3 81708 concentration of IgE an
Page 839 and 840:
GNEM 82844 immunoglobulin E (IgE)-s
Page 841 and 842:
GPEP 82623 2 0.70-3.49 Positive 3 3
Page 843 and 844:
GRHMS 50037 proteins) followed by r
Page 845 and 846:
9814 9815 ABO_M 9012 FGHBP 91958 an
Page 847 and 848:
FGCU 57482 GGUM 82479 Patients with
Page 849 and 850:
GUIN 82706 1 0.35-0.69 Equivocal 2
Page 851 and 852:
HIBS 83261 HAKE 82348 Haemophilus i
Page 853 and 854:
HALO 80339 4 17.5-49.9 Strongly pos
Page 855 and 856:
HAPT 9168 Virus (SNV), which causes
Page 857 and 858:
FHDLS 90186 FHE4 57164 proteins) fo
Page 859 and 860:
ingestion, whereas MMA and DMA are
Page 861 and 862:
HMSU 8633 HMSRU 60236 Reference val
Page 863 and 864:
SHELA 84409 SHELP 84407 MERCURY 0-1
Page 865 and 866:
SHELM 84408 is a convenient, noninv
Page 867 and 868:
HELM 82749 disease, low-grade gastr
Page 869 and 870: HLLFH 34854 5434 molecular prognost
Page 871 and 872: HHEMO 81508 States are homozygous f
Page 873 and 874: A2F 83341 A1c (HbA1c) is a result o
Page 875 and 876: HBF 8269 usually easily identified
Page 877 and 878: SDEX 9180 Clinical Information: The
Page 879 and 880: HAPB 80297 stomatocytes, polychroma
Page 881 and 882: FIXMS 84209 HQ 9220 Hemophilia B, F
Page 883 and 884: FHPCF 91658 HIT 81904 preparations
Page 885 and 886: FHVP 90406 HAVM 8342 patients treat
Page 887 and 888: HAVAB 32110 result indicates immuni
Page 889 and 890: HBIS 209102 Core Antibody, IgM, Ser
Page 891 and 892: HBABT 87893 appear. It is detectabl
Page 893 and 894: HBAGP 86185 HBAG 9013 Instructions.
Page 895 and 896: QHBV 82416 serum (after it had beco
Page 897 and 898: HEAG 8311 remains detectable for se
Page 899 and 900: HCVPS 13009 Clinical References: 1.
Page 901 and 902: HCV 80190 "but >69,000,000 IU/mL" i
Page 903 and 904: HCVQU 83142 Interpretations: Quanti
Page 905 and 906: HCCAD 87858 HCVG 81618 Hepatitis C
Page 907 and 908: FHED 91850 FHEPD 91335 FHEVG 91222
Page 909 and 910: HEPS 200830 Reference Values: HEPAT
Page 911 and 912: FHER2 81954 Treat 1997 43:87-95. Mo
Page 913 and 914: 81504 60198 tumors.(1) Specimens wi
Page 915 and 916: ACVK 89393 available to dimerize wi
Page 917 and 918: HHTM 89587 approximately 50% of dia
Page 919: HNPCC 17073 overall incidence of HH
Page 923 and 924: MHSV 87998 Clinical Information: He
Page 925 and 926: HSV 84422 Coombs RW, Benedetti J, e
Page 927 and 928: FHHV6 91311 FHV6D 57484 FHP6 80419
Page 929 and 930: FHART 57462 FHEXA 91442 HEXAI 82397
Page 931 and 932: NAGT 8776 Clinical References: 1. T
Page 933 and 934: y 4 years. Tay-Sachs disease is an
Page 935 and 936: NAGR 82943 TOTAL Reference values h
Page 937 and 938: FHSTW 57368 HMAX 5338 HIS 80944 Age
Page 939 and 940: HBRP 60213 antibodies is presumptiv
Page 941 and 942: RHIV 84455 Reference Range: Negativ
Page 943 and 944: HV1CM 60357 verified by submitting
Page 945 and 946: GHIV 82340 HIV, as well as nonviabl
Page 947 and 948: PHIV 88635 genotypic mutations pres
Page 949 and 950: limit of this assay. A "Detected" r
Page 951 and 952: HIVQU 81958 susceptibility to the s
Page 953 and 954: WBAR 23878 suspected or repeat HIV
Page 955 and 956: HIV2 86702 patients reside. A negat
Page 957 and 958: FHLAA 91498 FHLAB 91499 FHLA 91833
Page 959 and 960: HL15O 60348 HLA57 89346 An interpre
Page 961 and 962: LY27B 9648 HMBSS 61216 histocompati
Page 963 and 964: HCYSP 80379 in 350,000 live births.
Page 965 and 966: HVA 9253 HVAR 60275 Interpretation:
Page 967 and 968: HBV 82551 Class IgE kU/L Interpreta
Page 969 and 970: HORS 82874 immune response to aller
Page 971 and 972:
HSPR 82134 4 17.5-49.9 Strongly pos
Page 973 and 974:
DP 82904 Useful For: Testing for Ig
Page 975 and 976:
HDG 82906 HDHS 82903 Clinical Refer
Page 977 and 978:
FHUAB 57246 FHAMA 57151 THCG 80678
Page 979 and 980:
HHV6V 89888 HHV8 81971 Clinical Ref
Page 981 and 982:
80172 significance" (ASCUS) on Pap
Page 983 and 984:
needles. Two diseases are known to
Page 985 and 986:
FHIME 91376 Reference Values: Negat
Page 987 and 988:
SEROTYPE 3 (3) mcg/mL SEROTYPE 9 (9
Page 989 and 990:
FHYCO 90110 FHYCD 91637 HYMP 9736 N
Page 991 and 992:
FVIST 90121 HMDP 89220 Adults 8:00
Page 993 and 994:
HYOX 86213 CD19+ CD27+ IgM+ IgD+ 1.
Page 995 and 996:
SAL 8768 Aspergillus fumigatus #6 A
Page 997 and 998:
HIF2A 61681 61207 Interpretation: U
Page 999 and 1000:
FIFAF 91181 FSAGA 90047 X-linked di
Page 1001 and 1002:
FIGBP 57131 FIGF2 80758 16- or =18
Page 1003 and 1004:
CASF 8271 16- or =18 years: 341-894
Page 1005 and 1006:
IMPR 8126 CMPD. These translocation
Page 1007 and 1008:
FICP 91173 FISP 91624 C3, NEPH REFE
Page 1009 and 1010:
FIMM 91507 IGA 8157 urine protein e
Page 1011 and 1012:
IGE 8159 FLCP 84190 features, respo
Page 1013 and 1014:
BCGR 83123 BCGBM 31141 9-
Page 1015 and 1016:
IGM 8158 IGGS4 84250 Immunoglobulin
Page 1017 and 1018:
IMMG 8156 KAPPA TOTAL LIGHT CHAIN
Page 1019 and 1020:
MONOS 9081 IBDP 81443 Salt Lake Cit
Page 1021 and 1022:
SFLA 8169 SFLB 8175 Influenza Virus
Page 1023 and 1024:
FLUAB 60551 Influenza Virus Type A
Page 1025 and 1026:
INHAB 86336 INHA 81049 > or =16 yea
Page 1027 and 1028:
phase decline in FSH levels. Inhibi
Page 1029 and 1030:
INAB 8666 6 > or =100 Strongly posi
Page 1031 and 1032:
IGFP 83357 Clinical References: Thr
Page 1033 and 1034:
15 years 236-1,060 153 16 years 227
Page 1035 and 1036:
80 years 53-162 Reference values ha
Page 1037 and 1038:
acromegaly or gigantism in individu
Page 1039 and 1040:
IGFB3 83300 46-50 years 91-246 51-5
Page 1041 and 1042:
FINTE 90483 31-35 years: 3.5-7.0 mc
Page 1043 and 1044:
OIL28 61701 3-fold greater rates of
Page 1045 and 1046:
FIL2R 90021 FINL6 91979 FIL8 91654
Page 1047 and 1048:
IODU 8639 IOD 81574 ICRU 60440 Corr
Page 1049 and 1050:
FEU 8571 FET 8350 Reference Values:
Page 1051 and 1052:
FEUR 88970 FECRU 60764 A: Hemochrom
Page 1053 and 1054:
BTITH 8972 IHDI 82773 Clinical Info
Page 1055 and 1056:
ITDT 82775 concentration of IgE ant
Page 1057 and 1058:
ISPG 82768 ITCON 81247 newborn scre
Page 1059 and 1060:
JMACK 82819 0 Negative 1 0.35-0.69
Page 1061 and 1062:
JAK2B 88715 chronic myelogenous leu
Page 1063 and 1064:
JAK2V 31156 JCEDR 82865 Buser AS, e
Page 1065 and 1066:
FJCV 91827 81107 Reference Values:
Page 1067 and 1068:
JOHN 82900 symptoms, Raynaudâ€s
Page 1069 and 1070:
FKAL 88540 FKAN 90069 Results are e
Page 1071 and 1072:
89027 KIDBN 82619 Reference Values:
Page 1073 and 1074:
KITAS 88802 Interpretation: The int
Page 1075 and 1076:
88957 88955 dysphagia. Clin Cancer
Page 1077 and 1078:
FXYM 86374 immune response to aller
Page 1079 and 1080:
GALCK 60695 between 3 to 6 months o
Page 1081 and 1082:
FLACO 57111 LD_I 8679 receptor-targ
Page 1083 and 1084:
Interpretation: Marked elevations i
Page 1085 and 1086:
LAMQ 82682 LAMB 82699 Positive 4 >
Page 1087 and 1088:
LBC 60450 utilizing the platelet ch
Page 1089 and 1090:
LANG 82349 FLTX 57118 Langust (Lobs
Page 1091 and 1092:
LEADO 300115 recognized as a risk f
Page 1093 and 1094:
PBU 8600 produced for nondomestic u
Page 1095 and 1096:
PBHA 8495 PBNA 89857 standards for
Page 1097 and 1098:
LCATD 83253 C, Buchet JP, Leroyer A
Page 1099 and 1100:
LEGI 8204 estimated to be responsib
Page 1101 and 1102:
LEGRP 89564 LEIS 86219 elevated as
Page 1103 and 1104:
LEPD 82849 antibodies interact with
Page 1105 and 1106:
LETT 82805 Useful For: As an aid in
Page 1107 and 1108:
LLPT 19499 LAD1 81155 Leukemia/Lymp
Page 1109 and 1110:
LID 8382 FLIMB 91635 LIME 82360 0.2
Page 1111 and 1112:
LIND 82862 LINS 86311 Linden, IgE C
Page 1113 and 1114:
FLIPR 90347 LPS 8328 BFLAC 34622 LP
Page 1115 and 1116:
LPAWS 89005 Low HDL: or =60 mg/dL
Page 1117 and 1118:
FLPA2 57353 LMPP 83673 would be >5
Page 1119 and 1120:
FLIS 90717 TRIGLYCERIDES Normal: o
Page 1121 and 1122:
LKM 80387 LOB 82744 Product Monogra
Page 1123 and 1124:
FLCA 60619 8-Hydroxyloxapine: Refer
Page 1125 and 1126:
LUPPR 83092 LH 8663 Test Performed
Page 1127 and 1128:
9861 9956 PBORR 80574 Follicular: 2
Page 1129 and 1130:
FBBIA 91898 FBBAB 91309 Serology is
Page 1131 and 1132:
CLYWB 83857 FBBC6 91899 after onset
Page 1133 and 1134:
CLYME 83856 diagnosis. Useful For:
Page 1135 and 1136:
LPAGF 60592 Maximum proliferation o
Page 1137 and 1138:
LPMGF 60591 recognition. Chem Rev 1
Page 1139 and 1140:
FLCM 90042 LSDU 81743 birth to old
Page 1141 and 1142:
deficiency of sphingomyelinase, whi
Page 1143 and 1144:
LYZKM 60720 amyloidosis, with renal
Page 1145 and 1146:
FMNUT 91661 MACE 82492 Reference Va
Page 1147 and 1148:
MCRPL 87843 MGFT 60030 6 > or =100
Page 1149 and 1150:
MGF 81345 MGRU 60245 diuretics) enh
Page 1151 and 1152:
MGCRU 60244 Useful For: Magnesium l
Page 1153 and 1154:
MAL 9240 MAAN 82396 Plasmodium spec
Page 1155 and 1156:
MAND 82352 sensitization to particu
Page 1157 and 1158:
isocitrate dehydrogenase. It circul
Page 1159 and 1160:
MNS 8413 MNCRU 60027 Manganese, Pla
Page 1161 and 1162:
MBL 81051 1 0.35-0.69 Equivocal 2 0
Page 1163 and 1164:
MARE 82141 changes in behavior, dif
Page 1165 and 1166:
9828 MCC 88636 9230 6 > or =100 Str
Page 1167 and 1168:
MFOX 82914 immune response to aller
Page 1169 and 1170:
ME2KM 89285 with a clinical diagnos
Page 1171 and 1172:
MCADK 83934 acylcarnitines (ACRN/82
Page 1173 and 1174:
MELAI 82724 FMELT 57120 MELN Melale
Page 1175 and 1176:
This assay was developed and its pe
Page 1177 and 1178:
FMCPC 57437 Reference Range: Negati
Page 1179 and 1180:
Diagnosis of infections of the cent
Page 1181 and 1182:
levels found in CSF, passive transf
Page 1183 and 1184:
symptoms. The presence of mumps IgG
Page 1185 and 1186:
MEPHS 83778 FMERC 91120 HGOM 82755
Page 1187 and 1188:
HGHAR 8498 in 3 ways: -Hg(+2) is re
Page 1189 and 1190:
MESQ 82776 METAF 83006 Mesquite, Ig
Page 1191 and 1192:
PMET 81609 13-17 years: 57-286 mcg/
Page 1193 and 1194:
nonepisodic hypertension Interpreta
Page 1195 and 1196:
MTDNS 83131 undergoing treatment wi
Page 1197 and 1198:
METR 9322 MEVP 84159 sulfhemoglobin
Page 1199 and 1200:
FMMD 57307 MMAAF 81921 Methsuximide
Page 1201 and 1202:
MMAS 80289 Useful For: Evaluating c
Page 1203 and 1204:
MAHKM 89135 Clinical Information: M
Page 1205 and 1206:
MHDKM 61098 Carrier screening in ca
Page 1207 and 1208:
FMI2 57186 RMA 81260 been shown for
Page 1209 and 1210:
MPSF 82515 whether this needs to be
Page 1211 and 1212:
MTBS 81507 leucovorin (LV). These f
Page 1213 and 1214:
PMLK 82827 0 Negative 1 0.35-0.69 E
Page 1215 and 1216:
AMA 8176 Clinical Information: Here
Page 1217 and 1218:
MLH1H 87978 Usual therapeutic doses
Page 1219 and 1220:
MLHKM 83002 hereditary defective mi
Page 1221 and 1222:
MCDMS 89830 and endometrial cancer.
Page 1223 and 1224:
MOLD1 81878 MINT 61696 MOLU 89271 M
Page 1225 and 1226:
MOLPS 89270 appetite, tachycardia,
Page 1227 and 1228:
FMNM 91829 124 healthy adults by Ma
Page 1229 and 1230:
identification of a monoclonal band
Page 1231 and 1232:
MPSU 8823 considered an adequate sc
Page 1233 and 1234:
MDCG 86880 MORP 83132 SPSM 9184 Mon
Page 1235 and 1236:
MOTH 82738 FMOT 90157 Chapter 53, P
Page 1237 and 1238:
MOUS 82707 MOSP 82792 Mouse Epithel
Page 1239 and 1240:
9832 MPLB 89776 0 Negative 1 0.35-0
Page 1241 and 1242:
MSH2M 83016 mutation is identified
Page 1243 and 1244:
MSH6M 83723 instability and immunoh
Page 1245 and 1246:
9831 MCIV 85321 MPSSC 84464 Mucicar
Page 1247 and 1248:
MPSQN 81473 dysostosis multiplex, f
Page 1249 and 1250:
MUG 82683 allergic reactions to ins
Page 1251 and 1252:
MENKM 81082 MENMS 80573 Multiple En
Page 1253 and 1254:
FMUMM 91456 CMUMP 81435 0-4 months:
Page 1255 and 1256:
MMPM 80977 (meningitis/encephalitis
Page 1257 and 1258:
FMUSK 91445 MSTD 82801 6 > or =100
Page 1259 and 1260:
FHIST 90018 FHSAG 90017 FHSU 90019
Page 1261 and 1262:
MGEP 83371 the Lambert-Eaton myasth
Page 1263 and 1264:
MGLES 83369 Negative AChR GANGLIONI
Page 1265 and 1266:
CTBBL 82443 FMC12 91558 Useful For:
Page 1267 and 1268:
MTBPZ 56099 QTBG 83896 Interpretati
Page 1269 and 1270:
MGRP 60755 MHRP 60756 overimmunosup
Page 1271 and 1272:
FMPAB 90055 MPC 80422 FMPD 91429 FM
Page 1273 and 1274:
FMDS 84387 FMFC 60405 Test Performe
Page 1275 and 1276:
MYH 84304 MCA 9746 MYH Gene Analysi
Page 1277 and 1278:
MYOS 9035 MYOU 9274 Single titers o
Page 1279 and 1280:
FMYO 91544 FCHOP 84456 Reference Va
Page 1281 and 1282:
NAT2O 60345 hepatitis, peripheral n
Page 1283 and 1284:
FNTPX 57308 mast-cell activity, suc
Page 1285 and 1286:
NARC 82026 NKCP 28562 Test Performe
Page 1287 and 1288:
6-11 months: 31-56%* 12-23 months:
Page 1289 and 1290:
MGRNA 61646 Test Performed By Medto
Page 1291 and 1292:
FNMEN 91669 FNEOM 90288 (eg, cultur
Page 1293 and 1294:
NEURF 88846 FNMYC 87862 Reference V
Page 1295 and 1296:
Clinical Information: Paraneoplasti
Page 1297 and 1298:
FNEA 57115 NEEVP 84162 utilizing PN
Page 1299 and 1300:
NMOER 60796 for neuromyelitis optic
Page 1301 and 1302:
NSESF 81796 Clinical References: 1.
Page 1303 and 1304:
FNTSM 91940 DISCLAIMER required by
Page 1305 and 1306:
FNIAC 91379 NIU 8626 Reference Valu
Page 1307 and 1308:
NIS 8622 NICRU 60442 Environmental
Page 1309 and 1310:
NICOU 82510 Interpretation: Serum n
Page 1311 and 1312:
NPDKM 61116 NPD mutations in indivi
Page 1313 and 1314:
NPCKM 83118 NPCMS 89015 abnormal me
Page 1315 and 1316:
NITU 8586 NMDCS 61516 muscle protei
Page 1317 and 1318:
FNMR 91959 imaging (MRI) of pelvis,
Page 1319 and 1320:
SSF1 87294 NSIP 31769 NRDZ 501030 N
Page 1321 and 1322:
NEREG 31767 NORT 81858 Cypress, CA
Page 1323 and 1324:
54 years: 10-67 pg/mL 55 years: 10-
Page 1325 and 1326:
NPM1 89292 should be considered. Wh
Page 1327 and 1328:
OAK 82673 immune response to allerg
Page 1329 and 1330:
OCC2 81870 4 17.5-49.9 Strongly pos
Page 1331 and 1332:
OLIG 8017 OLIGO 84340 402 W. County
Page 1333 and 1334:
OLIVF 86306 4 17.5-49.9 Strongly po
Page 1335 and 1336:
OPATU 8473 semisynthetic narcotic d
Page 1337 and 1338:
OPRMO 60352 haplotype-based approac
Page 1339 and 1340:
OREG 82496 caused by the release of
Page 1341 and 1342:
IDENT 9221 ANIDE 8114 terms only. W
Page 1343 and 1344:
UOSMB 9257 UOSMF 9258 hematuria, re
Page 1345 and 1346:
FRAG 9064 OSCAL 80579 dehydration,
Page 1347 and 1348:
OVAL 82826 Low High Premenopausal
Page 1349 and 1350:
DOXA 61644 proteins) followed by re
Page 1351 and 1352:
OXU 8669 of oxalate can be increase
Page 1353 and 1354:
OXYCS 83654 P50 9110 Oxycodone ng/m
Page 1355 and 1356:
SQUI 82821 This test was developed
Page 1357 and 1358:
PAIN 86328 drugs of abuse. Opiate c
Page 1359 and 1360:
PAPN 82383 Useful For: Detection of
Page 1361 and 1362:
PARAV 80421 immunoglobulin E (IgE)-
Page 1363 and 1364:
PNEOE 80013 NEURONAL AND MUSCLE CYT
Page 1365 and 1366:
PARID 9202 OAP 9216 reported as "un
Page 1367 and 1368:
PTH2P 28380 levels, who have either
Page 1369 and 1370:
PTHFN 61526 Females 0-11 months: no
Page 1371 and 1372:
PCAB 83728 when tumors secrete PTHr
Page 1373 and 1374:
POFF 82549 PARO 83731 Laboratory Me
Page 1375 and 1376:
FPDF 91577 FPDM 91576 PARV 84325 Cl
Page 1377 and 1378:
PARVP 86337 host.(2,3) Infection wi
Page 1379 and 1380:
PCBP 80587 88905 indicated for use
Page 1381 and 1382:
88958 89672 PDGFRA, Mutation Analys
Page 1383 and 1384:
FPEAG 91999 FPEA4 91981 Interpretat
Page 1385 and 1386:
PEC 82880 bronchospasm) in infants
Page 1387 and 1388:
PAS3 83345 PAS8 83347 6 > or =100 S
Page 1389 and 1390:
PENG 80134 immunoglobulin E (IgE)-s
Page 1391 and 1392:
FFTAL 90099 PENTS 8239 Clinical Inf
Page 1393 and 1394:
9840 9839 PNPC 5341 ACASM 83632 Not
Page 1395 and 1396:
PERS 82353 UPH24 84047 Persimmon, I
Page 1397 and 1398:
FPHAI 91629 PCPUG 9788 PCPMC 89069
Page 1399 and 1400:
FPGT 91757 FPFUZ 91755 FPHIV 91756
Page 1401 and 1402:
FPEMA 90102 PHYF 6794 Conversion Fo
Page 1403 and 1404:
P_PB 8643 PNY 8604 Clinical Referen
Page 1405 and 1406:
FPHAB 57371 FPHOS 57310 ACLIP 86179
Page 1407 and 1408:
CLPMG 82976 2006;4: 295-306 5. Font
Page 1409 and 1410:
GCLIP 80993 15.0-39.9 APL (weakly p
Page 1411 and 1412:
PPL 8296 cross-linking beta 2 GP1 m
Page 1413 and 1414:
PMMIL 89656 Interpretation: Normal
Page 1415 and 1416:
PHBF 8029 RPOU 84007 POU 8526 West
Page 1417 and 1418:
PANH 81156 6 >or =100 Strongly posi
Page 1419 and 1420:
SPB 8892 PDRP 82796 Laboratory Meth
Page 1421 and 1422:
PINE 82381 PNAP 82815 Pine Nut, IgE
Page 1423 and 1424:
PIPU 81248 Clinical Information: Pi
Page 1425 and 1426:
PIOR 82851 FPIV 91493 Pityrosporum
Page 1427 and 1428:
PCPRO 61654 therefore, is an advers
Page 1429 and 1430:
FPCPD 83358 PLHBB 9096 Plasma Cell
Page 1431 and 1432:
FPACT 91760 PSGN 9079 Hemostasis an
Page 1433 and 1434:
PLUM 82809 drugs Interpretation: Ef
Page 1435 and 1436:
FPMP 91590 PMS2S 61173 Clinical Ref
Page 1437 and 1438:
FPNEU 91656 PNRP 81698 Long-range P
Page 1439 and 1440:
POLIO 80420 FPOLS 91469 GAAMS 89898
Page 1441 and 1442:
FPLWH 91991 POPSD 82632 Hirschhorn
Page 1443 and 1444:
PORK 82700 PBGDW 31894 Clinical Ref
Page 1445 and 1446:
PBGU 82068 Useful For: Confirmation
Page 1447 and 1448:
PEE 88886 a detailed interpretation
Page 1449 and 1450:
FQPPS 81652 UROPORPHYRIN < or =2 mc
Page 1451 and 1452:
counseling of the patient regarding
Page 1453 and 1454:
oth coproporphyrin and PBG excretio
Page 1455 and 1456:
FPOS 91997 POSA 89591 with lesser i
Page 1457 and 1458:
NAK 8468 dehydrogenase (LCHAD) defi
Page 1459 and 1460:
KBF 8028 KF 8375 Potassium, Body Fl
Page 1461 and 1462:
KUR 8527 FPOTW 92002 with rapid K i
Page 1463 and 1464:
PALB 9005 FPRGA 57110 17PRN 88646 R
Page 1465 and 1466:
10-12 years: 19-220 ng/dL 13-15 yea
Page 1467 and 1468:
FPAP2 91198 Reference Values: CHILD
Page 1469 and 1470:
Units: ng/dL Age Range Premature (2
Page 1471 and 1472:
PHESP 9021 products (ie, blood tran
Page 1473 and 1474:
PTRE 82784 adjustment based on bloo
Page 1475 and 1476:
detectable within 2 to 4 hours afte
Page 1477 and 1478:
FPROG 90287 GRNMS 89188 *Lippe BM,
Page 1479 and 1480:
PRLPM 84462 Clinical Information: P
Page 1481 and 1482:
PROCT 83097 PHD2 61683 prolactin le
Page 1483 and 1484:
FIBDD 57459 FPLAC 91783 FPMET 91564
Page 1485 and 1486:
FPROP 90362 FPPOX 57140 FPRSG 57149
Page 1487 and 1488:
FPSAP 91775 PSA 9284 Prostate Speci
Page 1489 and 1490:
PSAFT 81944 > or =80 < or =7.2 Fema
Page 1491 and 1492:
PROT 82139 CFX 9339 of pretreatment
Page 1493 and 1494:
S_FX 80775 Clinical Information: Ph
Page 1495 and 1496:
factors Va and VIIIa. In addition,
Page 1497 and 1498:
TPBF 8420 RPTU 85681 accurately ass
Page 1499 and 1500:
PTU 8261 PR3 82965 Interpretation:
Page 1501 and 1502:
PT 9236 C, protein S, or antithromb
Page 1503 and 1504:
PPFE 8739 Noncomplexed (free) proto
Page 1505 and 1506:
PCHES 8518 (0%-20%) and usually low
Page 1507 and 1508:
FPTH 90182 PT1K 89464 9236 ABRAHAM
Page 1509 and 1510:
PTP22 89315 PTPN11 are missense mut
Page 1511 and 1512:
PUSE 82362 Clinical References: 1.
Page 1513 and 1514:
FPYTH 91667 FPYD 90281 PLP 60295 >
Page 1515 and 1516:
PK 8659 of PDHC deficiency is a def
Page 1517 and 1518:
QFP 83149 Reference Values: 0.08-0.
Page 1519 and 1520:
ovarian granulosa cells and testicu
Page 1521 and 1522:
FQUET 91727 QUIN 8302 REPII 82782 C
Page 1523 and 1524:
RSER 82544 0 Negative 1 0.35-0.69 E
Page 1525 and 1526:
RASE 82366 Reference Values: Report
Page 1527 and 1528:
RASP 86305 Interpretation: Treatmen
Page 1529 and 1530:
RTUP 82794 proteins) followed by re
Page 1531 and 1532:
SORR 82737 Clinical Information: Cl
Page 1533 and 1534:
UREDF 83255 4986 1 0.35-0.69 Equivo
Page 1535 and 1536:
88501 PRA 8060 Clinical References:
Page 1537 and 1538:
SRSV 8301 RSVAN 110300 and Thrombos
Page 1539 and 1540:
RTIC 9108 FREB 90331 RBP24 81783 Mu
Page 1541 and 1542:
FRFSF 57516 RHUT 9060 RHNI 82856 Rh
Page 1543 and 1544:
RIBAV 60536 VITB2 61637 Ribavirin,
Page 1545 and 1546:
FRCBP 57342 Useful For: Testing for
Page 1547 and 1548:
RNAP 83397 myeloproliferative disea
Page 1549 and 1550:
ROTA 8886 MARS 82701 Test Performed
Page 1551 and 1552:
RB 8172 ROSC 80262 1 0.35-0.69 Equi
Page 1553 and 1554:
ROC 5194 ROM Reference Values: Nega
Page 1555 and 1556:
RYEG 82908 proteins) followed by re
Page 1557 and 1558:
F100B 57349 AASCA 83022 6 > or =100
Page 1559 and 1560:
SALC 8480 SALM 82754 Salicylate, Se
Page 1561 and 1562:
SARD 82818 sensitization to particu
Page 1563 and 1564:
SCALS 82259 SHUR 60451 Scallop, IgE
Page 1565 and 1566:
SCL70 80178 OXK 8148 SEAFP 31770 Sc
Page 1567 and 1568:
SECOS 8243 FSEC 90173 sensitization
Page 1569 and 1570:
SEUR 60077 Teratogenic effects are
Page 1571 and 1572:
FER 81641 Clinical Information: Sel
Page 1573 and 1574:
FSMN 91449 SEPTK 61101 clinical man
Page 1575 and 1576:
screening has a higher detection ra
Page 1577 and 1578:
directly into the amniotic fluid ca
Page 1579 and 1580:
HTR2O 60338 genotype.(4) - For the
Page 1581 and 1582:
HTTO 60339 (SSRIs) Evaluating patie
Page 1583 and 1584:
SERWB 84373 elevated in nearly all
Page 1585 and 1586:
can release 5-HT from EC-cells. Onc
Page 1587 and 1588:
SESA 82728 SHBG 9285 Sesame Seed, I
Page 1589 and 1590:
FSRY 88537 Reference ranges for pre
Page 1591 and 1592:
Class IgE kU/L Interpretation 0 Neg
Page 1593 and 1594:
SCADK 83947 sensitization and clini
Page 1595 and 1596:
FSHOX 57127 FSHRP 91650 SHRI 82677
Page 1597 and 1598:
BIR 82674 and to define the allerge
Page 1599 and 1600:
SIRO 81768 SM 81358 Following a sin
Page 1601 and 1602:
FSMS 88534 SMA 6284 Quantitative re
Page 1603 and 1604:
NAFT 60032 NABF 8039 NAF 8374 2007
Page 1605 and 1606:
NACCL 81692 NAU 8525 Clinical Refer
Page 1607 and 1608:
FSLA 91610 STFR 84283 Laboratory Me
Page 1609 and 1610:
FSOMA 90172 associated with statins
Page 1611 and 1612:
SOY 82886 SPAG 8980 Soybean, IgE Le
Page 1613 and 1614:
SAAS 89882 SAAI 89883 questioned. T
Page 1615 and 1616:
SPIN 86312 FSMAC U/g of cellular pr
Page 1617 and 1618:
FSCA2 91586 FSCA3 91587 FSCA6 91588
Page 1619 and 1620:
SFGP 83679 SPRU 82394 Clinical Refe
Page 1621 and 1622:
SQUID 82631 FSRP 57187 Clinical Ref
Page 1623 and 1624:
SSB 81359 with childhood LE, neonat
Page 1625 and 1626:
ST2S 61723 signs. The severity of i
Page 1627 and 1628:
FSTS 88539 Clinical Information: Cl
Page 1629 and 1630:
INSEC 31765 STBY 82676 Clinical Ref
Page 1631 and 1632:
SPNC 89971 SPNEU 83150 Although the
Page 1633 and 1634:
concentrations of IgG antibodies to
Page 1635 and 1636:
FSTRP 90440 FSTSC 91984 STR 8746 J
Page 1637 and 1638:
FSAI 57313 STCH 9928 FSTYR 91094 Ge
Page 1639 and 1640:
SDHSP 89550 Useful For: Evaluation
Page 1641 and 1642:
SDHKM 89554 is higher than that of
Page 1643 and 1644:
SDHSB 89551 When such correlations
Page 1645 and 1646:
SDHSD 89553 this subtype. SDHD show
Page 1647 and 1648:
FSUCC 57460 9849 9850 FSUGR 91989 S
Page 1649 and 1650:
SFZ 8238 identify allergens which m
Page 1651 and 1652:
SUNFS 82813 SUNF 82615 IgG < 1500 >
Page 1653 and 1654:
adiopaque stone, for whom stone ana
Page 1655 and 1656:
oral potassium citrate will raise t
Page 1657 and 1658:
SNS 82594 Supplemental Newborn Scre
Page 1659 and 1660:
5581 SGUM 82483 Note: This test is
Page 1661 and 1662:
VERG 82909 SWORD 82346 Company, 200
Page 1663 and 1664:
83361 SS18-SSX2 fusion. Unfortunate
Page 1665 and 1666:
SGSU 81035 the risks of systemic ad
Page 1667 and 1668:
SYPGN 32184 of reverse screening re
Page 1669 and 1670:
TBNY 82589 results of the first tre
Page 1671 and 1672:
TCIPF 60590 3-5 months: 170-830 cel
Page 1673 and 1674:
ABSOLUTE COUNTS CD45 Lymph Count, F
Page 1675 and 1676:
0-2 months: 6-32%* 3-5 months: 11-4
Page 1677 and 1678:
TCMPF 60588 T- and B-Cell Quantitat
Page 1679 and 1680:
TBBS 9336 2-5 years: 700-2,200 cell
Page 1681 and 1682:
CD45 Lymph Count, Flow 0-17 years:
Page 1683 and 1684:
FRTLP 89040 89041 Clinical Referenc
Page 1685 and 1686:
during the process of TCR rearrange
Page 1687 and 1688:
TCGR 83122 > or =55 years: >78 copi
Page 1689 and 1690:
TCP 89319 Useful For: Determining w
Page 1691 and 1692:
CD8+CD45RO+ memory T cells 2-26% of
Page 1693 and 1694:
Foxp3+CD4+CD25+ T cells and provide
Page 1695 and 1696:
FRT3P 600915 FRT3 9404 fluctuations
Page 1697 and 1698:
TUP 81792 Interpretation: Triiodoth
Page 1699 and 1700:
T4TF 8684 T4 8724 salicylates. Inte
Page 1701 and 1702:
TARR 82486 HEXMS 89278 Tarragon, Ig
Page 1703 and 1704:
TSD 82588 Interpretation: An interp
Page 1705 and 1706:
FFTEM 80763 TTBS 80065 TEST PERFORM
Page 1707 and 1708:
esponse. Bioavailable (TTBS/80065):
Page 1709 and 1710:
in SHBG (#9285 "Sex Hormone Binding
Page 1711 and 1712:
TTFB 83686 variable. Tanner stage V
Page 1713 and 1714:
Reference Values: TESTOSTERONE, TOT
Page 1715 and 1716:
associated with increased luteinizi
Page 1717 and 1718:
FFTEN 57102 THCU 8898 Reference Val
Page 1719 and 1720:
TGF1 89459 beta R-I, propagating th
Page 1721 and 1722:
TGF2 89461 (TAAD), which involves c
Page 1723 and 1724:
THEVP 84158 TLU 8603 Thalassemia an
Page 1725 and 1726:
FFTHC 90094 THEO 8661 1 gram. Usefu
Page 1727 and 1728:
TDP 85753 of sera from patients wit
Page 1729 and 1730:
83343 High Risk HPV DNA Detection:
Page 1731 and 1732:
83342 with HPV effect -High-grade s
Page 1733 and 1734:
TPMT 80291 Synonym(s): Pentothal Hy
Page 1735 and 1736:
FFTAT 91200 THRMP 83093 The thrombi
Page 1737 and 1738:
RTEP 89507 allergic reactions to in
Page 1739 and 1740:
TAP 89506 1 month-17 years: 170.0-1
Page 1741 and 1742:
12-23 months: 2,100-6,200 cells/mcL
Page 1743 and 1744:
TGAB 84382 Thyroglobulin Antibody,
Page 1745 and 1746:
HTG1 83069 This cutoff has been val
Page 1747 and 1748:
STSH 8939 in Special Instructions.
Page 1749 and 1750:
TPO 81765 associated with neonatal
Page 1751 and 1752:
TBGI 9263 TBPE 8838 relevant in wom
Page 1753 and 1754:
FFTIK 91818 TICKS 83265 Useful For:
Page 1755 and 1756:
FFTLA 91951 TIMG 82891 Reference Va
Page 1757 and 1758:
TTGA 82587 Genetic susceptibility i
Page 1759 and 1760:
TTGG 83660 Tissue Transglutaminase
Page 1761 and 1762:
TIS 89367 Clinical Information: Tit
Page 1763 and 1764:
TOBAC 82620 creatinine in a patient
Page 1765 and 1766:
TOBT 81594 FHIPP 91121 FFTLB 91141
Page 1767 and 1768:
TOPI 81546 Reference Values: Class
Page 1769 and 1770:
should be drawn and tested. Rubella
Page 1771 and 1772:
FFTIH 91594 Negative CMV IgM result
Page 1773 and 1774:
TOXOG 8267 amniotic fluid specimens
Page 1775 and 1776:
PTOX 81795 FFTXG 91211 FFTXM INTERP
Page 1777 and 1778:
FFTRA 91693 TNFN 300205 Company, 20
Page 1779 and 1780:
TACIF 84388 Transmembrane Activator
Page 1781 and 1782:
FFTRC 91091 TRZ 9624 Useful For: Id
Page 1783 and 1784:
TREE3 81704 sensitivity to inhalant
Page 1785 and 1786:
FFTPG 57315 FHAL 90119 STRIC 9017 F
Page 1787 and 1788:
TRVI 82853 Trichloroethylene, Blood
Page 1789 and 1790:
TRICY 500509 bronchospasm) in infan
Page 1791 and 1792:
TGLBF 61647 TRIG 8316 DOXEPIN AND N
Page 1793 and 1794:
FFTRM 90115 TMP 80146 SURM 80463 5
Page 1795 and 1796:
FFTRP 91774 inherited neurodegenera
Page 1797 and 1798:
WHIPB 87974 bacilli. Culture of Whi
Page 1799 and 1800:
CHAG 86159 bronchospasm) in infants
Page 1801 and 1802:
TRYPT 81608 TRYPP 82955 measurable
Page 1803 and 1804:
RTRPP 88546 Inborn Errors of Metabo
Page 1805 and 1806:
TURKF 82824 proteins) followed by r
Page 1807 and 1808:
FFTUR 92005 TRYPI 82848 6 > or =100
Page 1809 and 1810:
UBEKM 89920 UGTK Reference Values:
Page 1811 and 1812:
UGT2 89611 II; CN type I does not r
Page 1813 and 1814:
UGTI 89397 UGTIO 60349 UDP-Glucuron
Page 1815 and 1816:
U1A1O 60343 when predicting the UGT
Page 1817 and 1818:
FURA 90316 Clinical Information: Un
Page 1819 and 1820:
FURBF 57373 RURCU 89846 urealyticum
Page 1821 and 1822:
URCU 8529 RUA 9308 > or =16 years:
Page 1823 and 1824:
UMIC 9316 Reference Values: Descrip
Page 1825 and 1826:
UPGD 8599 Reference Values: 1.0-3.0
Page 1827 and 1828:
60714 tumor suppressor gene). The U
Page 1829 and 1830:
FVPA 81771 patients with uveal mela
Page 1831 and 1832:
VUR 89680 VS 83396 Useful For: Dete
Page 1833 and 1834:
VANPK 80141 VANCR 81749 Interpretat
Page 1835 and 1836:
VRERP 84406 VANIL 82621 Therapy, Ma
Page 1837 and 1838:
VMA 9454 VMAR 60274 HVA
Page 1839 and 1840:
FVZVS 91685 SVZP 84424 are at risk
Page 1841 and 1842:
LVZV 81241 FVEGF 91765 VIP 8150 Neg
Page 1843 and 1844:
VENLA 83732 Clinical Information: C
Page 1845 and 1846:
VLCKM 60037 VIBC 89658 Clinical Ref
Page 1847 and 1848:
VISCS 8168 VAE 60299 diagnosis by i
Page 1849 and 1850:
VITA 60298 FB12 9156 Health and Dis
Page 1851 and 1852:
B12 9154 FVITB 57319 FB12V 7. Benoi
Page 1853 and 1854:
B6PRO 61064 FBIOT 91902 VITE Vitami
Page 1855 and 1856:
VLTB 89190 the single most importan
Page 1857 and 1858:
VLTU 8826 VHLD Toxic concentration:
Page 1859 and 1860:
VHLSP 89083 Hes FJ, Hoppener JWM, L
Page 1861 and 1862:
9862 VWD2N 81662 contrast, nonsense
Page 1863 and 1864:
VWAG 9051 Useful For: Diagnosis of
Page 1865 and 1866:
VWPR 83099 Inherited vWD has been c
Page 1867 and 1868:
FVORI 91998 VORI 88698 FPIKE 91662
Page 1869 and 1870:
WARFP 60529 immune response to alle
Page 1871 and 1872:
WARFO 60341 impaired. Reference Val
Page 1873 and 1874:
9943 WSPV 82659 useful for evaluati
Page 1875 and 1876:
WEED2 81883 immune response to alle
Page 1877 and 1878:
WEED4 81885 4 17.5-49.9 Strongly po
Page 1879 and 1880:
WNVP 87802 Clinical Information: We
Page 1881 and 1882:
WEEPC 83918 WEEP 83156 virus: a pri
Page 1883 and 1884:
FWHET 91652 FWHT4 91978 sensitizati
Page 1885 and 1886:
ASHW 82730 sensitization and clinic
Page 1887 and 1888:
WFHV 82658 WHIC 82719 6 > or =100 S
Page 1889 and 1890:
POTA 82710 sensitization to particu
Page 1891 and 1892:
WSLK 82772 sensitivity to inhalant
Page 1893 and 1894:
WDKM 83698 Willow, IgE Clinical Inf
Page 1895 and 1896:
FWHS 88535 WORM 82680 2008;47(6):20
Page 1897 and 1898:
XHIM 82964 present (eg, 45,X/46,XX)
Page 1899 and 1900:
FBMT 80601 FXYLP 90359 XX/XY in Opp
Page 1901 and 1902:
YMICR 82992 FYSTG 92000 0-16 years:
Page 1903 and 1904:
FYERS 57374 ZAP70 83727 clinical ma
Page 1905 and 1906:
ZNU 8591 ZNRU 60526 lead-poisoning
Page 1907 and 1908:
ZNCRU 60527 ingestion relates to th
Page 1909:
FZUCE 92006 ZYG 81252 4. Kawada K,
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