3 CASES OF 45,X/46,XYNF MOSAICISM MOLECULAR ANALYSIS REVEALED HETEROGENEITY OF THE NONFLUORESCENT Y-CHROMOSOME

被引：16

作者：

GANSHIRTAHLERT, D

PAWLOWITZKI, IH

GAL, A

机构：

[1] UNIV MUNSTER,INST HUMAN GENET,VESALIUSWEG 12-14,D-4400 MUNSTER,FED REP GER

[2] UNIV BONN,INST HUMAN GENET,D-5300 BONN,FED REP GER

来源：

HUMAN GENETICS | 1987年 / 76卷 / 02期

关键词：

D O I：

10.1007/BF00284913

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：153 / 156

页数：4

共 25 条

[1] UNUSUAL SCARCITY OF RESTRICTION SITE POLYMORPHISM IN THE HUMAN THYROGLOBULIN GENE - A LINKAGE STUDY SUGGESTING AUTOSOMAL DOMINANCE OF A DEFECTIVE THYROGLOBULIN ALLELE [J].

BAAS, F ;

BIKKER, H ;

VANOMMEN, GJB ;

DEVIJLDER, JJM .

HUMAN GENETICS, 1984, 67 (03) :301-305

[2] REPEATED SEQUENCE SPECIFIC TO HUMAN MALES [J].

COOKE, H .

NATURE, 1976, 262 (5565) :182-186

[3]

DISTECHE CM, 1986, AM J HUM GENET, V38, P751

[4] SMALL DELETIONS OF THE SHORT ARM OF THE Y-CHROMOSOME IN 46,XY FEMALES [J].

DISTECHE, CM ;

CASANOVA, M ;

SAAL, H ;

FRIEDMAN, C ;

SYBERT, V ;

GRAHAM, J ;

THULINE, H ;

PAGE, DC ;

FELLOUS, M .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (20) :7841-7844

[5] X-LINKED DOMINANT CHARCOT-MARIE-TOOTH DISEASE - SUGGESTION OF LINKAGE WITH A CLONED DNA-SEQUENCE FROM THE PROXIMAL XQ [J].

GAL, A ;

MUCKE, J ;

THEILE, H ;

WIEACKER, PF ;

ROPERS, HH ;

WIENKER, TF .

HUMAN GENETICS, 1985, 70 (01) :38-42

[6]

GAL A, 1987, IN PRESS AM J HUM GE

[7] HAE-III RESTRICTION OF DNA FROM 3 CASES WITH NONFLUORESCENT Y-CHROMOSOMES (45XO/46XYNF) [J].

GANSHIRT, D ;

PAWLOWITZKI, IH .

HUMAN GENETICS, 1984, 67 (03) :241-244

[8]

GUELLAN G, 1984, NATURE, V207, P172

[9] A DNA FRAGMENT FROM THE HUMAN X-CHROMOSOME SHORT ARM WHICH DETECTS A PARTIALLY HOMOLOGOUS SEQUENCE ON THE Y-CHROMOSOMES LONG ARM [J].

KOENIG, M ;

CAMERINO, G ;

HEILIG, R ;

MANDEL, JL .

NUCLEIC ACIDS RESEARCH, 1984, 12 (10) :4097-4109

[10]

LUKUSA T, 1986, CLIN GENET, V29, P311

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