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The Principles of Clinical Cytogenetics - Extra Materials - Springer

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568 Index<br />

Cutaneous anaplastic large cell lymphoma<br />

(C-ALCL), t369, 405<br />

CVS (see Chorionic villus sampling)<br />

CYP17, t251<br />

CYP19, t251<br />

Cystic fibrosis, 544<br />

and congenital bilateral absence <strong>of</strong><br />

vas deferens (CBAVD), t254<br />

and hyperechoic bowel, 299, 300, t300<br />

and male infertility, t254<br />

Cystic hygroma, 291, 554<br />

<strong>Cytogenetics</strong>, origin <strong>of</strong> term, 3<br />

Cytokinesis, 21<br />

Cyt-µ, 386<br />

D<br />

DAPI, 74<br />

DAPI/DA staining, 74<br />

Database, 96<br />

DAX1, 226<br />

DAZ, 259<br />

DBY, 259<br />

De novo rearrangements, 167,168, 169–170,<br />

188, 191, 193, 195, 199, 200<br />

DEB, 351<br />

Degeneracy <strong>of</strong> the DNA code, 13<br />

DEK, 384, t388<br />

DEK/CAN, 384, t388<br />

del (X)(p21), 225<br />

del (X)(p22), 225<br />

del(5q), f374, t378<br />

in AML, 380, 383<br />

in ET, 374<br />

in MDS, 376<br />

in RAEB, 378<br />

in RCMD, 378<br />

syndrome, t368, f374, 379<br />

del(6q), f374, 393, 403<br />

del(7q), f374, t378, t388<br />

in AML, 380<br />

in CIMF, 373<br />

in RAEB, 378<br />

del(9)(p21),471<br />

del(9p), f374, 393<br />

del(9q), f374, 380<br />

del(11)(q22.3-q23.1), 473, f474<br />

del(11q), 395–396<br />

del(11q), f374, t389<br />

del(12p), f374, t390<br />

in aCML, 376<br />

in AML, 383<br />

in B-ALL, 393<br />

in T-PLL, 402<br />

del(13q), f374, t390, f470, 473, f473,<br />

f474, 475<br />

in CIMF, 373<br />

in CLL, 395, 396<br />

in ET, 373<br />

in MCL, 399<br />

in PV, 373<br />

in T-cell/NK cell neoplasms, 403<br />

del(16q), t391<br />

del(17p), 397, 399, 403<br />

del(20q), f374, t391<br />

in aCML, 376<br />

in ET, 373<br />

in PV, 373<br />

in RA, 376<br />

in RAEB, 378<br />

del(22q), 393<br />

Deleted in azoospermia (DAZ)/<br />

spermatogenesis on Y, 259<br />

Deletions, 45, 47, 165–167, f166, 168,<br />

169, 170, 171,172–175, f173, t176,<br />

178–180, f181, 184, f184, 185,<br />

189, 192, 197–198, 200<br />

benign, 172–173, 180, 181, 199<br />

contiguous gene syndromes, 174<br />

interstitial, 47, 167, 173–175, f173<br />

mechanism <strong>of</strong> formation, 165–167,<br />

f166, 170, 174–175, 178, 184<br />

nomenclature, 45, 47<br />

submicroscopic/microdeletions, 166–168,<br />

169, 171, 174–175<br />

telomere acquisition, 173-174<br />

terminal, 167, 173–174, f173<br />

X chromosome, 225<br />

and ovarian failure, 249, f250<br />

and primary amenorrhea, 249, f250

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