The Good SHP2 Association A Porthole Into the Genetics of Congenital Heart Disease

被引：3

作者：

Gelb, Bruce D. ^{[1
,2
,3
,6
]}

Seidman, Christine E. ^{[4
,5
]}

机构：

[1] Mt Sinai Sch Med, Child Hlth & Dev Inst, New York, NY 10029 USA

[2] Mt Sinai Sch Med, Dept Pediat, New York, NY 10029 USA

[3] Mt Sinai Sch Med, Dept Genet, New York, NY 10029 USA

[4] Harvard Univ, Sch Med, Howard Hughes Med Inst, Dept Genet, Boston, MA 02115 USA

[5] Brigham & Womens Hosp, Div Cardiovasc, Boston, MA 02115 USA

[6] Mt Sinai Sch Med, Dept Genom Sci, New York, NY 10029 USA

来源：

CIRCULATION-CARDIOVASCULAR GENETICS | 2012年 / 5卷 / 03期

关键词：

Editorials; heart defects; congenital; genetics; genome-wide analysis; genome-wide association study; tetralogy of Fallot; DEFECTS; LOCI;

D O I：

10.1161/CIRCGENETICS.112.963215

中图分类号：

R5 [内科学];

学科分类号：

100201 [内科学];

摘要：

[No abstract available]

引用

页码：271 / 273

页数：3

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