Mowat-Wilson syndrome and mutation in the zinc finger homeo box 1B gene: a well defined clinical entity

被引：32
|
作者：
Mainardi, PC
Pastore, G
Zweier, C
Rauch, A
机构：
[1] Osped S Andrea Vercelli, Div Pediat, Serv Genet, Dept Pediat, I-13100 Vercelli, Italy
[2] Osped S Andrea Vercelli, Genet Unit, I-13100 Vercelli, Italy
[3] Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, Germany
来源：
JOURNAL OF MEDICAL GENETICS | 2004年 / 41卷 / 02期
关键词：
D O I：
10.1136/jmg.2003.009548
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
[No abstract available]
引用
收藏
页数：6
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