Desmosterolosis presenting with multiple congenital anomalies and profound developmental delay.

被引：0
|
作者：
Andersson, HC
Kratz, LC
Kelley, RI
机构：
[1] Tulane Med Ctr, Human Genet Program, Hayward Gen Ctr, New Orleans, LA USA
[2] Kennedy Krieger Inst, Baltimore, MD USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2000年 / 67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：
131
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收藏
页码：36 / 36
页数：1
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