ANGELMAN SYNDROME IN A DAUGHTER WITH DEL(15) (Q11Q13) ASSOCIATED WITH BRACHYCEPHALY, HEARING-LOSS, ENLARGED FORAMEN MAGNUM, AND ATAXIA IN THE MOTHER

被引：34

作者：

WILLIAMS, CA

HENDRICKSON, JE

CANTU, ES

DONLON, TA

机构：

[1] STANFORD UNIV, MED CTR, DEPT GENET, STANFORD, CA 94305 USA

[2] UNIV FLORIDA, DIV HUMAN GENET, GAINESVILLE, FL 32611 USA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1989年 / 32卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320320312

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：333 / 338

页数：6

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