SISTER CHROMATID EXCHANGE IN DYSKERATOSIS CONGENITA LYMPHOCYTES

被引：46

作者：

BURGDORF, W ^{[1
]}

KURVINK, K ^{[1
]}

CERVENKA, J ^{[1
]}

机构：

[1] UNIV MINNESOTA,SCH DENT,DIV HUMAN & ORAL GENET,MINNEAPOLIS,MN 55455

来源：

JOURNAL OF MEDICAL GENETICS | 1977年 / 14卷 / 04期

关键词：

D O I：

10.1136/jmg.14.4.256

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：256 / 257

页数：2

共 12 条

[1] CHROMOSOME ABNORMALITIES IN CONSTITUTIONAL APLASTIC ANEMIA [J].

BLOOM, GE ;

WARNER, S ;

GERALD, PS ;

DIAMOND, LK .

NEW ENGLAND JOURNAL OF MEDICINE, 1966, 274 (01) :8-&

[2] MANIFOLD INCREASE IN SISTER CHROMATID EXCHANGES IN BLOOMS SYNDROME LYMPHOCYTES [J].

CHAGANTI, RS ;

SCHONBERG, S ;

GERMAN, J .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (11) :4508-4512

[3] SISTER CHROMATID EXCHANGE IN HUMAN CHROMOSOMES FROM NORMAL INDIVIDUALS AND PATIENTS WITH ATAXIA TELANGIECTASIA [J].

GALLOWAY, SM ;

EVANS, HJ .

CYTOGENETICS AND CELL GENETICS, 1975, 15 (01) :17-29

[4] RATE OF SISTER CHROMATID EXCHANGES PARALLEL TO SPONTANEOUS CHROMOSOME BREAKAGE IN FANCONIS ANEMIA AND TO TRENIMON-INDUCED ABERRATIONS IN HUMAN LYMPHOCYTES AND FIBROBLASTS [J].

HAYASHI, K ;

SCHMID, W .

HUMANGENETIK, 1975, 29 (03) :201-206

[5]

HOOK EB, 1975, PEDIATR RES, V9, P313

[6] GIEMSA TECHNIQUE FOR DETECTION OF SISTER CHROMATID EXCHANGES [J].

KORENBERG, JR ;

FREEDLENDER, EF .

CHROMOSOMA, 1974, 48 (04) :355-360

[7] INDUCTION BY ALKYLATING-AGENTS OF SISTER CHROMATID EXCHANGES AND CHROMATID BREAKS IN FANCONIS ANEMIA [J].

LATT, SA ;

STETTEN, G ;

JUERGENS, LA ;

BUCHANAN, GR ;

GERALD, PS .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (10) :4066-4070

[8]

MORRISON JG, 1974, S AFR MED J, V48, P223

[9] SPONTANEOUS CHROMOSOMAL ABERRATIONS IN FAMILY PANMYELOPATHY [J].

SCHROEDER, TM ;

ANSCHUTZ, F ;

KNOPP, A .

HUMANGENETIK, 1964, 1 (02) :194-196

[10] DYSKERATOSIS CONGENITA - CLINICAL FEATURES AND GENETIC ASPECTS - REPORT OF A FAMILY AND REVIEW OF LITERATURE [J].

SIRINAVIN, C ;

TROWBRIDGE, AA .

JOURNAL OF MEDICAL GENETICS, 1975, 12 (04) :339-354

← 1 2 →