Truncating loss-of-function mutations ofDISP1contribute to...

Human Genetics 2009 / 05 Vol. 125; Iss. 4

Truncating loss-of-function mutations ofDISP1contribute to holoprosencephaly-like microform features in humans

Erich Roessler, Yong Ma, Maia V. Ouspenskaia, Felicitas Lacbawan, Claude Bendavid, Christèle Dubourg, Philip A. Beachy, Maximilian Muenke
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Volume:
125
Language:
english
Pages:
8
DOI:
10.1007/s00439-009-0628-7
Date:
May, 2009
File:
PDF, 336 KB
english, 2009
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