FG SYNDROME

被引：30

作者：

THOMPSON, E

BARAITSER, M

机构：

来源：

JOURNAL OF MEDICAL GENETICS | 1987年 / 24卷 / 03期

关键词：

D O I：

10.1136/jmg.24.3.139

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

收藏

页码：139 / 143

页数：5

相关论文

共 9 条

[1] FG SYNDROME IN A PREMATURE MALE
BIANCHI, DW
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 19 (02): : 383 - 386
[2] 2 RETARDED MALE COUSINS WITH ODD FACIES, HYPOTONIA, AND SEVERE CONSTIPATION - POSSIBLE EXAMPLES OF THE X-LINKED FG-SYNDROME
BURN, J
MARTIN, N
[J]. JOURNAL OF MEDICAL GENETICS, 1983, 20 (02) : 97 - 99
[3] NEW SYNDROME OF MENTAL DEFICIENCY WITH CRANIOFACIAL, LIMB, AND ANAL ABNORMALITIES
KELLER, MA
JONES, KL
NYHAN, WL
FRANCKE, U
DIXSON, B
[J]. JOURNAL OF PEDIATRICS, 1976, 88 (04) : 589 - 591
[4] SENSORINEURAL DEAFNESS IN THE FG SYNDROME - REPORT ON 4 NEW CASES
NERI, G
BLUMBERG, B
MILES, PV
OPITZ, JM
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 19 (02): : 369 - 377
[5] STUDIES OF MALFORMATION SYNDROMES OF MAN XXXIII - FG SYNDROME - X-LINKED RECESSIVE SYNDROME OF MULTIPLE CONGENITAL ANOMALIES AND MENTAL-RETARDATION
OPITZ, JM
KAVEGGIA, EG
[J]. ZEITSCHRIFT FUR KINDERHEILKUNDE, 1974, 117 (01): : 1 - 18
[6] STUDIES OF MALFORMATION SYNDROMES OF HUMANS .67. THE FG SYNDROME - FURTHER-STUDIES ON 3 AFFECTED INDIVIDUALS FROM THE FG FAMILY
OPITZ, JM
KAVEGGIA, EG
ADKINS, WN
GILBERT, EF
VISESKUL, C
PETTERSEN, JC
BLUMBERG, B
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 12 (02): : 147 - 154
[7] FG SYNDROME - FURTHER CHARACTERIZATION, REPORT OF A 3RD FAMILY, AND OF A SPORADIC CASE
RICCARDI, VM
HASSLER, E
LUBINSKY, MS
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1977, 1 (01): : 47 - 58
[8] THOMPSON EM, 1985, CLIN GENET, V27, P582
[9] NECROPSY FINDINGS IN A CHILD WITH FG SYNDROME
THOMPSON, EM
HARDING, BN
LAKE, BD
SMITH, SC
[J]. JOURNAL OF MEDICAL GENETICS, 1986, 23 (04) : 372 - 373