The Principles of Clinical Cytogenetics - Extra Materials - Springer

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Index 565 abnormality previous, and risk of recurrence, 304 structural, and mosaicism, 311 analysis, 77–79 band, 29, 31 banding pattern, first report of, 6 breakage, f1, 3471348 breakage syndrome, 350 dicentric, 48 instability acentric fragment, 351 chromatid breaks, 351 chromosome end fusion, 351 chromosome lag, 354 dicentric fragment, 351 endoreduplicated chromosomes, 351 gaps, 351 micronuclei, 354 multiradial configuration, 354 multiradial formation, 351 quadriradial configuration, 356 rings, 351 syndrome, 347, 350 in situ hybridization, 53 isodicentric, 48 landmarks, 31 marker, 49 nomenclature, 27, 28 origin of term, 3 paint , 55 Philadelphia, 52 pseudodicentric, 48 region, 29, 31 ring, 33, 49 structure, 15–17 sub-band, 31 unknown origin, 44 Chromosome 2 mosaicism, in amniotic fluid cells, t308, t310, t311 trisomy, in cultured chorionic villus preparations, 286 Chromosome 3 mosaicism, in amniotic fluid cells, t308, t310, t311 trisomy, in direct chorionic villus preparations, 286 Chromosome 4 mosaicism, in amniotic fluid cells, t308, 310, t311 Chromosome 5 mosaicism, in amniotic fluid cells, t308, 310, t311 Chromosome 6 mosaicism, in amniotic fluid cells, t308, 310, t311 Chromosome 7 mosaicism, in amniotic fluid cells, t308, t310, t311 trisomy, in direct chorionic villus preparations, 286 Chromosome 8 mosaic trisomy, in chorionic villus preparations, 287 mosaicism, in amniotic fluid cells, 307, 308, t308, 310, t311 Chromosome 9 monosomy, 310 mosaicism, in amniotic fluid cells, t308, 310, t311 Chromosome 11 mosaicism, in amniotic fluid cells, t308, 310, t311 Chromosome 12 mosaicism, in amniotic fluid cells, t308, 309, 310, t311 Chromosome 13 mosaicism, in amniotic fluid cells, 308, 309, 310 Chromosome 14 mosaicism, in amniotic fluid cells, t308, 310, t311 Chromosome 15 and uniparental disomy, 285, 286 mosaicism, in amniotic fluid cells, t308, 310, t311 Chromosome 16
566 Index mosaicism, in amniotic fluid cells, 308, t308, 309, 310, t311 mosaicism, in chorionic villus cells, 310 Chromosome 17 monosomy, 310 mosaicism, in amniotic fluid cells, t308, 310, t311 Chromosome 18 mosaicism, in amniotic fluid cells, 308, 310 Chromosome 19 monosomy, 310 mosaicism, in amniotic fluid cells, t308, 310, t311 Chromosome 20 monosomy, 310 mosaicism, in amniotic fluid cells, 309, 310 Chromosome 21 monosomy, 310 mosaicism, in amniotic fluid cells, 308, 310 Chromosome 22 monosomy, 310 mosaicism, in amniotic fluid cells, t308, 310, t311 Chromosome 22q11.2 microdeletion and heart defects, 292, 293, t293 and extracardiac defects, t293 Chromosomes acrocentric, 74 rodent, 73 Chronic eosinophilic leukemia (CEL), t368, 373 Chronic idiopathic myelofibrosis (CIMF), t368, 373 Chronic lymphocytic leukemia (CLL), t368, 395, t469, 473, t473, f474 17p13, 473, f474 ATM , 473, f474 del(11)(q22.3-q23.1), 473, f474 del(13)(q14), f470, 473, f474 TP53, 473, f474 trisomy 12, 473, f474 Chronic myelogenous leukemia (CML), 367, 370, 372-373, 469, t469, f471, f472, 545 Abelson (ABL) oncogene, 469, f471, f472 argininosuccinate synthetase gene (ASS), 470, f471 atypical, 375–376 blast crisis, 370, t373 breakpoint cluster region (BCR) gene, 469, f471, f472 four color FISH (F-FISH), 470, f472 M-BCR, 370 m-BCR, 370 p210 , 370 p230, 370 Philadelphia rearrangement, 370 t(9;22), 366, 370, f371, 469, f470, f471, f472 Chronic myelomonocytic leukemia (CMML), t368, 375 Chronic myeloproliferative diseases (MPD), 367, t368 Chronic neutrophilic leukemia (CNL), t368, 373 Ciliary dyskinesia, primary, t255 CIMF, t368, 373 Classical Hodgkin lymphoma (CHL), t369, 407–408 Classical satellite probe, 456 Clear cell carcinoma, renal, 430–431, 438 Cleft palate, 248, 339 CLIA ’88, 94, 108 Clinical Laboratory Improvement Amendments (CLIA ’88), 94, 108 CLL, t368, 395 Clonal evolution, 51 Clone definition of, 51 evolution, 51 related, 51 size, 51 unrelated, 51 Clubfoot and mosaic trisomy 16, 310
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The Principles of Clinical Cytogene
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The Principles of Clinical Cytogene
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v Preface In the summer of 1989, on
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vii Preface to First Edition The st
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ix Contents Preface ...............
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Contributors SARAH HUTCHINGS CLARK,
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History of Clinical Cytogenetics 1
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4 Steven Gersen The hypotonic solut
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6 Steven Gersen marrow aspiration,
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8 Steven Gersen 9. Hsu, T.C. (1952)
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10 Martha Keagle Fig. 1. DNA struct
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12 Martha Keagle Fig. 3. Transcript
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14 Martha Keagle Fig. 5. Translatio
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16 Martha Keagle Fig. 7. The levels
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18 Martha Keagle single-copy DNA is
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20 Martha Keagle Fig. 10. Mitosis.
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22 Martha Keagle Fig. 11. Schematic
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24 Martha Keagle Fig. 13. Spermatog
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Human Chromosome Nomenclature 27 IN
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Human Chromosome Nomenclature 29 Fi
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Human Chromosome Nomenclature 33 Ta
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Human Chromosome Nomenclature 47 In
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Human Chromosome Nomenclature 49 Ma
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Human Chromosome Nomenclature 51 Un
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Human Chromosome Nomenclature 53 Ta
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Human Chromosome Nomenclature 55 46
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Human Chromosome Nomenclature 57 nu
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Basic Laboratory Procedures 59 II E
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Basic Laboratory Procedures 63 INTR
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Basic Laboratory Procedures 65 amni
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Basic Laboratory Procedures 67 Prep
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Basic Laboratory Procedures 69 Fig.
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Basic Laboratory Procedures 77 Lack
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Basic Laboratory Procedures 79 Once
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82 Christopher McAleer Fig. 1. Sche
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84 Christopher McAleer measurements
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86 Christopher McAleer allow light
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88 Christopher McAleer High-dry obj
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90 Christopher McAleer Fig. 3. Sche
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Quality Control and Quality Assuran
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Automation in the Cytogenetics Labo
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Autosomal Aneuploidy 131 III Clinic
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Autosomal Aneuploidy 133 INTRODUCTI
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135 Table 1 Parental and Meiotic/Mi
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Autosomal Aneuploidy 137 Fig. 2. Sc
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Autosomal Aneuploidy 139 forming ab
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Autosomal Aneuploidy 141 Fig. 5. Th
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Autosomal Aneuploidy 143 Fig. 6. Pr
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Autosomal Aneuploidy 145 Fig. 8. An
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Autosomal Aneuploidy 147 trisomies,
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Autosomal Aneuploidy 149 21 and ind
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Autosomal Aneuploidy 151 molecular
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Autosomal Aneuploidy 153 Fig. 10. T
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Autosomal Aneuploidy 155 This marke
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Autosomal Aneuploidy 157 47. Hawley
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Autosomal Aneuploidy 159 110. Lindo
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Autosomal Aneuploidy 161 171. Moghe
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Autosomal Aneuploidy 163 231. Reese
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Structural Chromosome Rearrangement
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177 Prader-Willi Paternal deletion
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179 Table 2 Some Recurring Duplicat
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Sex Chromosomes and Sex Chromosome
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Cytogenetics of Infertility 247 INT
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Cytogenetics of Infertility 249 Amo
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Cytogenetics of Infertility 251 Tab
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Cytogenetics of Infertility 253 gen
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255 Primary ciliary dyskinesia Auto
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Cytogenetics of Infertility 257 cha
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Cytogenetics of Infertility 259 Tab
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Cytogenetics of Infertility 261 Fig
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Cytogenetics of Infertility 263 rat
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Cytogenetics of Infertility 265 39.
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268 Linda Marie Randolph By 1986, m
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270 Linda Marie Randolph Table 1 Ch
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272 Linda Marie Randolph Table 4 Th
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274 Linda Marie Randolph Table 6 Fr
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276 Linda Marie Randolph rate of 14
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278 Table 8 Outcome in Early (11-14
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280 Linda Marie Randolph Table 9 Vo
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282 Linda Marie Randolph In 1995, O
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284 Linda Marie Randolph Fig. 1. Il
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286 Linda Marie Randolph reported c
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288 Linda Marie Randolph The underl
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290 Linda Marie Randolph Fig. 3. Ul
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296 Linda Marie Randolph Fig. 6. De
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298 Linda Marie Randolph Choroid Pl
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300 Linda Marie Randolph Table 13 C
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302 Linda Marie Randolph Table 14 U
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304 Linda Marie Randolph then that
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306 Table 15 Prenatal Results for R
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308 Linda Marie Randolph Table 17 O
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310 Linda Marie Randolph DNA marker
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312 Linda Marie Randolph XX and XY
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314 Linda Marie Randolph 54. Simpso
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316 Linda Marie Randolph 116. Wang,
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318 Linda Marie Randolph 173. Cicer
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320 Linda Marie Randolph 232. Benn,
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Cytogenetics of Spontaneous Abortio
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348 Xiao-Xiang Zhang Fig. 1. An exa
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350 Xiao-Xiang Zhang cases availabl
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352 Xiao-Xiang Zhang Fig. 2. Metaph
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354 Xiao-Xiang Zhang patients, grea
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356 Xiao-Xiang Zhang Fig. 5. G-Band
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358 Xiao-Xiang Zhang Fig. 7. Sister
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360 Xiao-Xiang Zhang REFERENCES 1.
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Cytogenetics of Hematologic Neoplas
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387 Table 5 Association of Recurren
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389 del(8)(q22) t(8;16)(p11.2;p13)
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391 +17 -17 2° assoc. with +21 i(1
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Cytogenetics of Solid Tumors 421 IN
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423 Aytpical (see well-differentiat
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Cytogenetics of Solid Tumors 425 So
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Cytogenetics of Solid Tumors 427 ca
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Cytogenetics of Solid Tumors 429 do
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Cytogenetics of Solid Tumors 431 cl
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Cytogenetics of Solid Tumors 433 Fi
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Cytogenetics of Solid Tumors 439 no
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Cytogenetics of Solid Tumors 441 ch
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Cytogenetics of Solid Tumors 445 8.
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Cytogenetics of Solid Tumors 447 64
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454 Daynna Wolff and Stuart Schwart
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Fragile X 491 VI Beyond Chromosomes
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Fragile X 495 18 Fragile X From Cyt
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Fragile X 497 Fig. 1. Appearance of
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Fragile X 499 Table 4 Characteristi
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Fragile X 501 (KH domains) and clus
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Fragile X 503 have suggested differ
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Fragile X 505 The premutation form
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Fragile X 507 Table 4). FRAXE expan
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Fragile X 509 35. Heitz, D., Devys,
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Fragile X 511 93. Bennetto, L. and
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Fragile X 513 147. Oostra, B.A. and
Page 531 and 532: 516 Jin-Chen Wang Fig. 1. Diagramma
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Page 551 and 552: 536 Jin-Chen Wang 138. Dryja, T.P.,
Page 553 and 554: 538 Jin-Chen Wang 192. Karanjawala,
Page 555 and 556: 540 Jin-Chen Wang 248. Creau-Goldbe
Page 557 and 558: 542 Sarah Hutchings Clark condition
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Page 563 and 564: 548 Sarah Hutchings Clark chromosom
Page 565 and 566: 550 Sarah Hutchings Clark SMITH-MAG
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Page 569 and 570: 554 Sarah Hutchings Clark The relat
Page 571 and 572: 556 Sarah Hutchings Clark Although,
Page 573 and 574: 558 Sarah Hutchings Clark 33. Nicol
Page 575 and 576: 560 Index Abnormalities, order of,
Page 577 and 578: 562 Index Anus, imperforate, 310 AP
Page 579: 564 Index CDK4, 394 CDK6, 396 CDKN2
Page 583 and 584: 568 Index Cutaneous anaplastic larg
Page 585 and 586: 570 Index proximal 15q, 178, t179 p
Page 587 and 588: 572 Index Folic acid pathway, 75 Fo
Page 589 and 590: 574 Index Hereditary neuropathy wit
Page 591 and 592: 576 Index Intrachromosomal recombin
Page 593 and 594: 578 Index Male-specific region, Y c
Page 595 and 596: 580 Index MTX, 76 Mucosa-associated
Page 597 and 598: 582 Index Octamer, 14 Okazaki fragm
Page 599 and 600: 584 Index Premature separation of s
Page 601 and 602: 586 Index Recombinant chromosomes n
Page 603 and 604: 588 Index Sézary syndrome (SS), t3
Page 605 and 606: 590 Index t(4;14), 475 t(5;10), 375
Page 607 and 608: 592 Index Treacher Collins syndrome
Page 609 and 610: 594 Index Xq deletions, 225 Y trans
Page 611 and 612: 596 Index XX males, 467, f468 and a
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