Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia

标题
Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia
作者
关键词
-
出版物
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 89, Issue 2, Pages 289-294
出版商
Elsevier BV
发表日期
2011-07-25
DOI
10.1016/j.ajhg.2011.06.007

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