VERIFICATION OF THE FETAL VALPROATE SYNDROME PHENOTYPE

被引：224

作者：

ARDINGER, HH

ATKIN, JF

BLACKSTON, RD

ELSAS, LJ

CLARREN, SK

LIVINGSTONE, S

FLANNERY, DB

PELLOCK, JM

HARROD, MJ

LAMMER, EJ

MAJEWSKI, F

SCHINZEL, A

TORIELLO, HV

HANSON, JW

机构：

[1] VIRGINIA COMMONWEALTH UNIV,MED COLL VIRGINIA,DEPT HUMAN GENET,RICHMOND,VA 23298

[2] VIRGINIA COMMONWEALTH UNIV,MED COLL VIRGINIA,DEPT NEUROL,DIV CHILD NEUROL,RICHMOND,VA 23298

[3] UNIV TEXAS,DEPT OBSTET & GYNECOL,DALLAS,TX 75230

[4] MASSACHUSETTS GEN HOSP,EMBRYOL TERATOL UNIT,BOSTON,MA 02114

[5] INST HUMAN GENET,DUSSELDORF,FED REP GER

[6] UNIV ZURICH,DEPT MED GENET,CH-8006 ZURICH,SWITZERLAND

[7] BLODGETT MEM MED CTR,GENET BIRTH DEFECTS NEUROL CLIN,GRAND RAPIDS,MI

[8] UNIV WASHINGTON,DEPT PEDIAT,SEATTLE,WA 98195

[9] UNIV VIRGINIA,DEPT PEDIAT,DIV MED GENET,CHARLOTTESVILLE,VA 22903

[10] EMORY UNIV,DEPT PEDIAT,DIV MED GENET,ATLANTA,GA 30322

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1988年 / 29卷 / 01期

关键词：

D O I：

10.1002/ajmg.1320290123

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：171 / 185

页数：15

共 31 条

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[J]. JOURNAL OF PEDIATRICS, 1981, 99 (05) : 828 - 828
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