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
    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