PHENOTYPIC VARIATION IN MALE-TRANSMITTED FRAGILE-X - GENETIC INFERENCES

被引：56

作者：

LOESCH, DZ

HAY, DA

SUTHERLAND, GR

HALLIDAY, J

JUDGE, C

WEBB, GC

机构：

[1] LA TROBE UNIV,DEPT GENET & HUMAN VARIAT,BUNDOORA,VIC 3083,AUSTRALIA

[2] ADELAIDE CHILDRENS HOSP,DEPT HISTOPATHOL,CYTOGENET UNIT,N ADELAIDE,SA 5006,AUSTRALIA

[3] ROYAL CHILDRENS HOSP,DEPT GENET,PARKVILLE,VIC 3052,AUSTRALIA

[4] ROYAL CHILDRENS HOSP,MURDOCH INST RES BIRTH DEFECTS,PARKVILLE,VIC 3052,AUSTRALIA

[5] WILLSEMERE HOSP,KEW,VIC,AUSTRALIA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 27卷 / 02期

关键词：

D O I：

10.1002/ajmg.1320270219

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：401 / 417

页数：17

共 29 条

[1]

COOPER B, 1981, ASSESSING HANDICAPS, P93

[2]

DAKER MG, 1981, LANCET, V1, P780

[3] TRANSMISSION OF THE MARKER-X SYNDROME TRAIT BY UNAFFECTED MALES - CONCLUSIONS FROM STUDIES OF LARGE FAMILIES [J].

FROSTERISKENIUS, U ;

SCHULZE, A ;

SCHWINGER, E .

HUMAN GENETICS, 1984, 67 (04) :419-427

[4] TRANSMISSION OF FRAGILE (X)(Q27) FROM NORMAL MALE(S) [J].

FRYNS, JP ;

VANDENBERGHE, H .

HUMAN GENETICS, 1982, 61 (03) :262-263

[5]

GARDNER RJM, 1983, CLIN GENET, V23, P311

[6] CONSIDERATION OF CONNECTIVE-TISSUE DYSFUNCTION IN THE FRAGILE-X SYNDROME [J].

HAGERMAN, RJ ;

VANHOUSEN, K ;

SMITH, ACM ;

MCGAVRAN, L .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 17 (01) :111-121

[7]

HAY DA, 1985, ESSENTIALS BEHAVIOUR, P234

[8]

HOWARDPEEBLES PN, 1985, AM J HUM GENET, V37, P956

[9] A CYTOGENETIC STUDY OF A POPULATION OF MENTALLY-RETARDED MALES WITH SPECIAL REFERENCE TO THE MARKER(X) SYNDROME [J].

JACOBS, PA ;

MAYER, M ;

MATSUURA, J ;

RHOADS, F ;

YEE, SC .

HUMAN GENETICS, 1983, 63 (02) :139-148

[10] COGNITIVE PROFILES AND THE SPECTRUM OF CLINICAL MANIFESTATIONS IN HETEROZYGOUS FRA(X) FEMALES [J].

KEMPER, MB ;

HAGERMAN, RJ ;

AHMAD, RS ;

MARINER, R .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (1-2) :139-156

← 1 2 3 →