INDIVIDUAL VARIATION AND SPECIFIC COGNITIVE DEFICITS IN THE FRA(X) SYNDROME

被引:62
作者
THEOBALD, TM
HAY, DA
JUDGE, C
机构
[1] LA TROBE UNIV,DEPT PSYCHOL,BUNDOORA,VIC 3083,AUSTRALIA
[2] LA TROBE UNIV,DEPT GENET & HUMAN VARIAT,BUNDOORA,VIC 3083,AUSTRALIA
[3] ST NICHOLAS HOSP,CARLTON,VIC,AUSTRALIA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 28卷 / 01期
关键词
D O I
10.1002/ajmg.1320280102
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:1 / 11
页数:11
相关论文
共 37 条
[1]   FRAGILE X-LINKED MENTAL-RETARDATION - A SURVEY OF 65 PATIENTS WITH MENTAL-RETARDATION OF UNKNOWN ORIGIN [J].
CARPENTER, NJ ;
LEICHTMAN, LG ;
SAY, B .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1982, 136 (05) :392-398
[2]  
DAKER MG, 1981, LANCET, V1, P780
[3]   THE FRAGILE X-SYNDROME - THE PATIENTS AND THEIR CHROMOSOMES [J].
DEARCE, MA ;
KEARNS, A .
JOURNAL OF MEDICAL GENETICS, 1984, 21 (02) :84-91
[4]   GENETICS OF SPECIFIC COGNITIVE-ABILITIES [J].
DEFRIES, JC ;
VANDENBERG, SG ;
MCCLEARN, GE .
ANNUAL REVIEW OF GENETICS, 1976, 10 :179-207
[5]   X-LINKED MENTAL-RETARDATION AND AN X-CHROMOSOME MARKER [J].
GERALD, PS .
NEW ENGLAND JOURNAL OF MEDICINE, 1980, 303 (12) :696-697
[6]  
GRAHAM JM, 1983, BEHAV GENET, V13, P536
[7]  
GUSTAVSON KH, 1981, CLIN GENET, V19, P101
[8]  
HAGERMAN RJ, 1983, FRAGILE X SYNDROME D, P83
[9]   THE LA-TROBE TWIN STUDY - A GENETIC APPROACH TO THE STRUCTURE AND DEVELOPMENT OF COGNITION IN TWIN CHILDREN [J].
HAY, DA ;
OBRIEN, PJ .
CHILD DEVELOPMENT, 1983, 54 (02) :317-330
[10]  
HAY DA, 1985, ESSENTIALS BEHAVIOUR