22q11 deletion syndrome and the role of the TBX1 transcription

被引：0
|
作者：
Scambler, PJ
Ivins, S
Ataliotis, P
Prescott, K
Latinkic, B
Mohun, T
Lindsay, E
Pramparo, T
Baldini, A
机构：
[1] MMU, Inst Child Hlth, London, England
[2] Natl Inst Med Res, Div Dev Biol, London NW7 1AA, England
[3] Baylor Coll Med, Dept Pediat Cardiol, Houston, TX 77030 USA
[4] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
来源：
JOURNAL OF MEDICAL GENETICS | 2002年 / 39卷
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：
SP24
引用
收藏
页码：S20 / S20
页数：1
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