Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1
出版年份 2012 全文链接
标题
Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1
作者
关键词
-
出版物
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 158A, Issue 3, Pages 574-580
出版商
Wiley
发表日期
2012-02-08
DOI
10.1002/ajmg.a.35217
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Hypoparathyroidism and autoimmunity in the 22q11.2 deletion syndrome
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- A patient with a de novo distal 22q11.2 microdeletion and anxiety disorder
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- 1.4Mb recurrent 22q11.2 distal deletion syndrome, two new cases expand the phenotype
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