Chromosome 22q11 deletion syndrome and sclerocornea in an infant boy.

被引：0
|
作者：
Raff, ML
Mitchell, AL
Robinson, W
Leppig, KA
Weiss, AH
机构：
[1] Childrens Hosp & Reg Med Ctr, Div Genet & Dev, Seattle, WA USA
[2] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[3] Univ Washington, Dept Med, Div Med Genet, Seattle, WA 98195 USA
[4] Univ British Columbia, Dept Med Genet, Vancouver, BC V5Z 1M9, Canada
[5] Grp Hlth Cooperat Puget Sound, Seattle, WA 98121 USA
[6] Univ Washington, Dept Ophthalmol, Seattle, WA 98195 USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2002年 / 71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：
564
引用
收藏
页码：268 / 268
页数：1
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