Exon resequencing, mutation detection, and copy number analysis in syndromic oesophageal atresia

被引：0
|
作者：
Storer, Mekayla [1 ]
Howard, E. [2 ]
Lefebvre, G. [2 ]
Martin, V. [1 ]
Coffey, A. [2 ]
Larsen, L. [3 ]
Tumer, Z. [3 ]
Bates, M. [4 ]
Wieczorek, D. [5 ]
Shaw-Smith, C. [1 ]
机构：
[1] Inst Child Hlth, London, England
[2] Wellcome Trust Sanger Inst, Cambridge, England
[3] Kennedy Ctr, Copenhagen, Denmark
[4] Cincinnati Childrens Hosp, Cincinnati, OH USA
[5] Inst Human Genet & Anthropol, Essen, Germany
来源：
JOURNAL OF MEDICAL GENETICS | 2008年 / 45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：
引用
收藏
页码：S50 / S50
页数：1
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