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J.AJHG.2014.01.001
J.AJHG.2014.01.001
http://dx.doi.org/10.1016/J.AJHG.2014.01.001
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects
P356
Q28306581-A6C5486B-8DCB-42E5-90A8-584C10BD625A
P356
J.AJHG.2014.01.001
http://dx.doi.org/10.1016/J.AJHG.2014.01.001