Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate

标题
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate
作者
关键词
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出版物
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 98, Issue 4, Pages 755-762
出版商
Elsevier BV
发表日期
2016-03-25
DOI
10.1016/j.ajhg.2016.02.013

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