Autosomal dominant Robinow syndrome in 11 affected family members: Marked phenotypic variability.

被引：0
|
作者：
Kostiner, D
Cox, V
Golabi, M
Hoyme, HE
机构：
[1] Univ Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA 94143 USA
[2] Stanford Univ, Dept Pediat, Div Genet, Stanford, CA 94305 USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2001年 / 69卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
690
引用
收藏
页码：301 / 301
页数：1
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