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304 Laboratorio de Genética: Genética Hereditaria Martínez Fernández AR, Fuentes Corripio I, Rodríguez Ferrer M, Domingo Fernández CJ. Toxoplasmosis. Medicine 1998; 81: 3760-6. Centers for Disease Control and Prevention. Sensivity of the test for antibody to hepatitis B surface antigen. Unites States. MMWR 1993; 42: 707-10. Grosheide PM, Wladimiroff JW, Heijtink RA, Mazel JA, Christiaens GCML, Nuijten ASM, et al. Proposal for routine antenatal screening at 14 weeks for hepatitis B surface antigen. BMJ 1995; 311 (4): 1197-9. Larsen SA, Kraus SJ, Winttington WL. Diagnostic test. En: Larsen SA, Hunter EF, Kraus SJ, EDS. A manual of test for syphilis. Washington DC. American Public Health Association, 1990. Zaaijer HL, Exel-Oehlrss PV, Kraaijeveld T, Altena E, Lelie PN. Early detection of antibodies to HIV-1 by third- generation assays. Lancet 1992; 340: 770-2. Ades AE, Sculpher MJ, Gibb DM, Gupta R, Ratcliffe J. Cost effectiveness analysis of antenatal HIV screening in United Kingdom. BMJ 1999; 319 (7219): 1230-4. Pareja Bezares A, Álvarez Pasquín MJ, Batalla Martínez C, Comín Bertrán E, Gómez Marco JJ, Niño Martín V, et al. Prevención de las enfermedades transmisibles. Atención Primaria 1999; 24 Suppl 1: 99-114. Gilson GJ, Christensen F, Romero H, Bekes K, Silva L, Qualls CR. Prevention of group B streptococcus early-onset neonatal sepsis: comparision of the Center for Disease Control and prevention screening-based protocol to a risk-based protocol in infants at greater than 37 week's gestation. J Perinatol 2000; 20 (8 Pt 1): 491-5. Montero Alonso R, Barbadillo Izquierdo F, Anso Olivan S, Marrero Calvo M, Carpintero Martín I, Sastre Huerta E, et al. Neonatal sepsis caused by Streptococcus agalactiae. What should be done? An Esp Pediatr 1998; 48 (3): 288-92. Group B stretococcal disease prevention practices of obstetrician-gynecologist. Obstet Gynecol 2001; 98 (1): 7-13. Cate S. Maternal serum triple analyte screening in pregnancy. Am Fam Phys 2000; 62 (4): 738-40. Taipale P, Hilesmaa V, Salonen R, Ylöstalo P. Increased nuchal translucency as a marker for fetal chromosomal defects. N Engl J Med 1997; 337: 1654-8. Programa atención a la mujer. Atención Primaria Insalud. Area 9. Madrid 1999. Vintzileos AM, Ananth CV, Fisher AJ, Smulian JC, Day-Salvatore D, Beazoglou T, et al. An economic evaluation of second trimester genetic ultrasonography for prenatal detection of down syndrome. Am J Obstet Gynecol 1998; 179: 1214-9. Kuppermann M, Goldberg JD, Nease RF, Washington AE. Who should be offered prenatal diagnosis? The 35-year old question. Am J Public Health. 1999; 89 (2): 160-3. Wald NJ, Watt HC, Hackshaw AK. Integrated screening for Down´s syndrome based on tests performed during the first and second trimesters. N Engl J Med 1999; 341: 461-7. Bricker L, Crowley P, Neilson J, O'Dowd T. Antenatal care of low risk pregnancies: ultrasound. Clinical Evidence 2000; 4: 781-92 (BMJ publishing group). Roberts T, Mugford M, Piercy J. Choosing options for ultrasound screening in pregnancy and comparision cost effectiveness: A decision analysis approach. Br J Obstet Gynaecol 1999; 106 (4): 397-8. Cusick W, Vintzileos AM. Fetal Down syndrome screening: a cost effectiveness analysis of alternative screening programs. J Matern Fetal Med 1999; 8 (6): 243-8.
Técnico Superior Sanitario de Laboratorio de Diagnóstico Clínico Vintzileos AM, Anauth CV, Smulian JC, Beazoglou T, Knupple RA. Routine second-trimester ultrasonography in United States: A cost-benefit analysis. Am J Obstet Gynecol 2000; 182 (3): 655-60. Hayashi M, Kozu H, Takei H. Maternal urinary free b-subunit of human corionic gonadotrophin: creatinine ratios and fetal chromosomal abnormalities in the second trimester of pregnancy. Br J Obstet Gynaecol 1996; 103: 577-80. Torgerson DJ. The impact of maternal age on the cost effectiveness of Down´s syndrome screening. Br J Obstet Gynaecol 1996; 103 (6): 581-3. Vintzileos AM, Anauth CV, Fisher AJ, Smulian JC, Day-Salvatore D, Beazoglou T, et al. An economic evaluation of prenatal strategies for detection of trisomy 18. Am J Obstet Gynecol 1998; 179 (5): 1220-4. Bach Vallmajor C. Diagnóstico prenatal: cribado serológico de malformaciones congénitas. JANO 2000; 58 (1333): 857-64. Ginecol Obstet Méx 2002; Vol. 70(12): 607-612 Fundació Santiago Dexeus Font, Medwave. Curso: Crecimiento, Desarrollo y Patologías del Feto y el Recién Nacido. Dr. Waldo Sepúlveda L., Departamento de Obstetricia y Ginecología, Especialidad Medicina Materno-Fetal, Clínica Los Condes Las causas del síndrome de Down. David Patterson. Investigación y Ciencia 133, 28-35 (1987) 10 Years of Genomics, Chromosome 21, and Down Syndrome. Stylianos E. Antonarakys (e-mail: Stylianos.Antonarakis@medecine.unige.ch). Genomics 51, 1-16 (1998) Article no. GE985335 Genética en medicina. Thompson y thompson 208 – 213 Hodes ME, Cole J, Palmer CG, Reed T. Clinical experience with trisomies 18 and 13. J Med Genet 1978; 15:48-60 Boghosian-Sell L, Mewar R, Harrison W, et al. Molecular mapping of the Edwards syndrome to two noncontiguous regions on chromosome 18. Am J Med Hum Genet 1994; 55:476-83 Marion RW, Chitayat D, Hutcheon G, et al. Trisomy 18 score: A rapid, reliable diagnostic test for trisomy 18. J Pediatr 1988; 113:45-8 Baty B, Blackburn B, Carey J. Natural history of trisomy 18 and 13: I. Growth, physical assessment, medical histories, survival and recurrence risk. Am J Med Genet 49:175-188, 1994 Baty B, Jorde L, Blackburn B, Carey J. Natural history of trisomy 18 and 13: II. Psychomotor Sotos JF. Genetic disorders associated with overgrowth. Clin Pediatr 1997; 36:39-49 Smyth CM, Bremner WJ. Klinefelter syndrome. Arch Intern Med 1998; 158:1309-1314 ASDOWN (Asociación de síndrome de Down Cádiz y bahía) Del cromosoma al gen. Corporación Sanitaria Clinic.Institut de Bioquímica Clinica 305
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LABORATORIO DE GENÉTICA: GENÉTICA
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INDICE UNIDAD TEMÁTICA I. Laborato
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Presentación, normas y procedimien
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Laboratorio de Genética: Genética
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Técnico Superior Sanitario de Labo
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1. LA CÉLULA Laboratorio de Genét
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5) Diacinesis Laboratorio de Genét
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Meiosis en el sexo femenino y mascu
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UNIDAD TEMÁTICA IV GENÉTICA HERED
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