Exome Sequencing Identifies a Recurrent De Novo ZSWIM6 Mutation Associated with Acromelic Frontonasal Dysostosis

Published 2014 View Full Article

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Title
Exome Sequencing Identifies a Recurrent De Novo ZSWIM6 Mutation Associated with Acromelic Frontonasal Dysostosis
Authors
Keywords
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Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 95, Issue 2, Pages 235-240
Publisher
Elsevier BV
Online
2014-08-07
DOI
10.1016/j.ajhg.2014.07.008

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