Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome

被引：59
|
作者：
Pinson, L
Augé, J
Audollent, S
Mattéi, G
Etchevers, H
Gigarel, N
Razavi, F
Lacombe, D
Odent, S
Le Merrer, M
Amiel, J
Munnich, A
Meroni, G
Lyonnet, S
Vekemans, M
Attié-Bitach, T
机构：
[1] Hop Necker Enfants Malad, Dept Genet, Paris, France
[2] Hop Necker Enfants Malad, INSERM, U393, Paris, France
[3] Hop Pellegrin Enfants, Serv Genet Med, Bordeaux, France
[4] Hop Pontchaillou, Serv Genet Med, Rennes, France
[5] Telethon Inst Genet & Med, Naples, Italy
来源：
JOURNAL OF MEDICAL GENETICS | 2004年 / 41卷 / 05期
关键词：
D O I：
10.1136/jmg.2003.014829
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
页码：381 / 386
页数：6
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