STUDIES OF MALFORMATION SYNDROMES OF HUMANS .67. THE FG SYNDROME - FURTHER-STUDIES ON 3 AFFECTED INDIVIDUALS FROM THE FG FAMILY

被引：30

作者：

OPITZ, JM

KAVEGGIA, EG

ADKINS, WN

GILBERT, EF

VISESKUL, C

PETTERSEN, JC

BLUMBERG, B

机构：

[1] CENT WISCONSIN CTR DEV DISABLED,MADISON,WI

[2] UNIV WISCONSIN,CTR HLTH SCI,SCH MED,DEPT PATHOL,MADISON,WI 53706

[3] UNIV WISCONSIN,CTR HLTH SCI,SCH MED,DEPT PEDIAT,MADISON,WI 53706

[4] UNIV WISCONSIN,CTR HLTH SCI,SCH MED,DEPT ANAT,MADISON,WI 53706

[5] UNIV CALIF LOS ANGELES,LOS ANGELES CTY HARBOR MED CTR,DEPT PEDIAT,TORRANCE,CA 90509

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1982年 / 12卷 / 02期

关键词：

D O I：

10.1002/ajmg.1320120205

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：147 / 154

页数：8

共 6 条

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COHEN, MM .

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[2] NEW SYNDROME OF MENTAL DEFICIENCY WITH CRANIOFACIAL, LIMB, AND ANAL ABNORMALITIES [J].

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JONES, KL ;

NYHAN, WL ;

FRANCKE, U ;

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JOURNAL OF PEDIATRICS, 1976, 88 (04) :589-591

[3] STUDIES OF MALFORMATION SYNDROMES OF MAN XXXIII - FG SYNDROME - X-LINKED RECESSIVE SYNDROME OF MULTIPLE CONGENITAL ANOMALIES AND MENTAL-RETARDATION [J].

OPITZ, JM ;

KAVEGGIA, EG .

ZEITSCHRIFT FUR KINDERHEILKUNDE, 1974, 117 (01) :1-18

[4]

OPITZ JM, 1976, J PEDIATR-US, V89, P687, DOI 10.1016/S0022-3476(76)80429-5

[5]

OPITZ JM, 1979, BIRTH DEFECTS COMPEN, P813

[6] FG SYNDROME - FURTHER CHARACTERIZATION, REPORT OF A 3RD FAMILY, AND OF A SPORADIC CASE [J].

RICCARDI, VM ;

HASSLER, E ;

LUBINSKY, MS .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1977, 1 (01) :47-58

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