GENETIC-LINKAGE HETEROGENEITY IN THE FRAGILE X-SYNDROME

被引：49

作者：

BROWN, WT

GROSS, AC

CHAN, CB

JENKINS, EC

机构：

来源：

HUMAN GENETICS | 1985年 / 71卷 / 01期

关键词：

D O I：

10.1007/BF00295659

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：11 / 18

页数：8

共 40 条

[1]

BROWN WT, 1981, LANCET, V2, P1055

[2] AUTISM IS ASSOCIATED WITH THE FRAGILE-X SYNDROME [J].

BROWN, WT ;

JENKINS, EC ;

FRIEDMAN, E ;

BROOKS, J ;

WISNIEWSKI, K ;

RAGUTHU, S ;

FRENCH, J .

JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 1982, 12 (03) :303-308

[3] CLOSE LINKAGE OF FRAGILE X MENTAL-RETARDATION SYNDROME TO HEMOPHILIA-B AND TRANSMISSION THROUGH A NORMAL-MALE [J].

CAMERINO, G ;

MATTEI, MG ;

MATTEI, JF ;

JAYE, M ;

MANDEL, JL .

NATURE, 1983, 306 (5944) :701-704

[4] INHERITED CONGENITAL NORMOFUNCTIONAL TESTICULAR HYPERPLASIA AND MENTAL DEFICIENCY [J].

CANTU, JM ;

SCAGLIA, HE ;

MEDINA, M ;

GONZALEZDIDDI, M ;

MORATO, T ;

MORENO, ME ;

PEREZPALACIOS, G .

HUMAN GENETICS, 1976, 33 (01) :23-33

[5]

CAVALLISFORZA LL, 1971, GENETICS HUMAN POPUL, P836

[6]

CHOO KH, 1984, LANCET, V2, P349

[7] CONSTITUTIVE FRAGILE SITES 1P31, 3P14, 6Q26, AND 16Q23 AND THEIR USE AS CONTROLS FOR FALSE-NEGATIVE RESULTS WITH THE FRAGILE(X) [J].

DANIEL, A ;

EKBLOM, L ;

PHILLIPS, S .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 18 (03) :483-491

[8]

DUNN HG, 1963, AM J MENT DEF, V67, P827

[9] 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

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

FRYNS, JP ;

VANDENBERGHE, H .

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

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