Genome-Wide Screen for Common and Rare Copy Number Variation in Metabolic Syndrome

被引：0
|
作者：
Kristiansson, Kati [1 ,2 ]
Barnes, Chris [1 ]
Perola, Markus [2 ]
Jula, Antti [2 ]
Salomaa, Veikko [2 ]
Ripatti, Samuli [2 ]
Hurles, Matthew [1 ]
Peltonen, Leena [1 ,2 ,3 ]
机构：
[1] Wellcome Trust Sanger Inst, Hinxton, England
[2] Natl Inst Hlth & Welf, Helsinki, Finland
[3] Broad Inst MIT & Harvard, Boston, MA USA
来源：
CIRCULATION | 2010年 / 122卷 / 02期
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D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
0381
引用
收藏
页码：E90 / E91
页数：2
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