CONSIDERATION OF CONNECTIVE-TISSUE DYSFUNCTION IN THE FRAGILE-X SYNDROME

被引:51
作者
HAGERMAN, RJ [1 ]
VANHOUSEN, K [1 ]
SMITH, ACM [1 ]
MCGAVRAN, L [1 ]
机构
[1] SEWALL REHABIL CTR,DENVER,CO
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1984年 / 17卷 / 01期
关键词
D O I
10.1002/ajmg.1320170106
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:111 / 121
页数:11
相关论文
共 16 条
[1]  
BRONSON E, 1918, BRIT J CHILD DIS, V15, P241
[2]   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
[3]   TREATMENT OF HOMOCYSTINURIA WITH PYRIDOXINE - A PRELIMINARY STUDY [J].
CARSON, NAJ ;
CARRE, IJ .
ARCHIVES OF DISEASE IN CHILDHOOD, 1969, 44 (235) :387-&
[4]   LINKAGE BETWEEN G6PD AND FRAGILE-X SYNDROME [J].
FILIPPI, G ;
RINALDI, A ;
ARCHIDIACONO, N ;
ROCCHI, M ;
BALAZS, I ;
SINISCALCO, M .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 15 (01) :113-119
[5]  
HARPEY JP, 1982, PEDIATRICS, V69, P670
[6]   HOMOCYSTINURIA CAUSED BY 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY - A CASE IN AN INFANT RESPONDING TO METHIONINE, FOLINIC ACID, PYRIDOXINE, AND VITAMIN-B12 THERAPY [J].
HARPEY, JP ;
ROSENBLATT, DS ;
COOPER, BA ;
LEMOEL, G ;
ROY, C ;
LAFOURCADE, J .
JOURNAL OF PEDIATRICS, 1981, 98 (02) :275-278
[7]   X-LINKED MENTAL-RETARDATION - A STUDY OF 7 FAMILIES [J].
JACOBS, PA ;
GLOVER, TW ;
MAYER, M ;
FOX, P ;
GERRARD, JW ;
DUNN, HG ;
HERBST, DS .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 7 (04) :471-489
[8]  
LEJEUNE J, 1982, LANCET, V1, P273
[9]  
McKusick V.A., 1972, CLIN GENET
[10]  
OPITZ JM, 1983, AM J MED GENET