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

页码：111 / 121

页数：11

共 16 条

[1] BRONSON E, 1918, BRIT J CHILD DIS, V15, P241
[2] INHERITED CONGENITAL NORMOFUNCTIONAL TESTICULAR HYPERPLASIA AND MENTAL DEFICIENCY
CANTU, JM
SCAGLIA, HE
MEDINA, M
GONZALEZDIDDI, M
MORATO, T
MORENO, ME
PEREZPALACIOS, G
[J]. HUMAN GENETICS, 1976, 33 (01) : 23 - 33
[3] TREATMENT OF HOMOCYSTINURIA WITH PYRIDOXINE - A PRELIMINARY STUDY
CARSON, NAJ
CARRE, IJ
[J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1969, 44 (235) : 387 - &
[4] LINKAGE BETWEEN G6PD AND FRAGILE-X SYNDROME
FILIPPI, G
RINALDI, A
ARCHIDIACONO, N
ROCCHI, M
BALAZS, I
SINISCALCO, M
[J]. 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
HARPEY, JP
ROSENBLATT, DS
COOPER, BA
LEMOEL, G
ROY, C
LAFOURCADE, J
[J]. JOURNAL OF PEDIATRICS, 1981, 98 (02) : 275 - 278
[7] X-LINKED MENTAL-RETARDATION - A STUDY OF 7 FAMILIES
JACOBS, PA
GLOVER, TW
MAYER, M
FOX, P
GERRARD, JW
DUNN, HG
HERBST, DS
[J]. 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