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

Published 2016 View Full Article

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Title
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate
Authors
Keywords
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Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 98, Issue 4, Pages 755-762
Publisher
Elsevier BV
Online
2016-03-25
DOI
10.1016/j.ajhg.2016.02.013

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