Prader-Willi syndrome phenotype in X chromosome anomalies: Evidence for a distinct syndrome

被引：0
|
作者：
Stratakis, CA
机构：
[1] NICHD, Unit Genet & Endocrinol, SPE, DEB,NIH, Bethesda, MD 20892 USA
[2] Georgetown Univ, Childrens Med Ctr, Dept Pediat, Washington, DC 20007 USA
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1998年 / 80卷 / 03期
关键词：
D O I：
10.1002/(SICI)1096-8628(19981116)80:3<294::AID-AJMG24>3.3.CO;2-6
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：294 / 295
页数：2
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