Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans

标题
Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans
作者
关键词
-
出版物
HUMAN GENETICS
Volume 125, Issue 4, Pages 393-400
出版商
Springer Nature
发表日期
2009-01-30
DOI
10.1007/s00439-009-0628-7

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