AUTISM IS ASSOCIATED WITH THE FRAGILE-X SYNDROME

被引:157
作者
BROWN, WT
JENKINS, EC
FRIEDMAN, E
BROOKS, J
WISNIEWSKI, K
RAGUTHU, S
FRENCH, J
机构
关键词
D O I
10.1007/BF01531375
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
引用
收藏
页码:303 / 308
页数:6
相关论文
共 23 条
[1]  
BROWN WT, 1981, LANCET, V2, P1055
[2]  
BROWN WT, 1982, LANCET, V1, P100
[3]   AUTISM IN CHILDREN WITH CONGENITAL RUBELLA [J].
CHESS, S .
JOURNAL OF AUTISM AND CHILDHOOD SCHIZOPHRENIA, 1971, 1 (01) :33-47
[4]   INFANTILE-AUTISM - GENETIC STUDY OF 21 TWIN PAIRS [J].
FOLSTEIN, S ;
RUTTER, M .
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES, 1977, 18 (04) :297-321
[5]  
FRIEDMAN E, 1969, SCHIZOPHRENIA, V1, P249
[6]   CONSTITUTIONAL CHROMOSOMAL BREAKAGE [J].
GIRAUD, F ;
AYME, S ;
MATTEI, JF ;
MATTEI, MG .
HUMAN GENETICS, 1976, 34 (02) :125-136
[7]  
GLOVER TW, 1981, AM J HUM GENET, V33, P234
[8]   FAMILIAL X-LINKED MENTAL-RETARDATION WITH AN X-CHROMOSOME ABNORMALITY [J].
HARVEY, J ;
JUDGE, C ;
WIENER, S .
JOURNAL OF MEDICAL GENETICS, 1977, 14 (01) :46-50
[9]   NONSPECIFIC X-LINKED MENTAL-RETARDATION .2. THE FREQUENCY IN BRITISH-COLUMBIA [J].
HERBST, DS ;
MILLER, JR .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 7 (04) :461-469
[10]   FRAGILE SITES IN HUMAN-CHROMOSOMES .2. DEMONSTRATION OF THE FRAGILE SITE XQ27 IN CARRIERS OF X-LINKED MENTAL-RETARDATION [J].
HOWARDPEEBLES, PN .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 7 (04) :497-501