Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome

出版年份 2011 全文链接

标题

Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome

作者

关键词

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出版物

AMERICAN JOURNAL OF HUMAN GENETICS

Volume 88, Issue 5, Pages 616-620

出版商

Elsevier BV

发表日期

2011-05-09

DOI

10.1016/j.ajhg.2011.04.005

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