Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects

标题
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
作者
关键词
-
出版物
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 106, Issue 1, Pages 26-40
出版商
Elsevier BV
发表日期
2019-12-20
DOI
10.1016/j.ajhg.2019.11.010

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