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J.AJHG.2012.11.015
J.AJHG.2012.11.015
http://dx.doi.org/10.1016/J.AJHG.2012.11.015
Exome sequencing identifies INPPL1 mutations as a cause of opsismodysplasia
P356
Q24307279-4116121F-634F-40DC-856A-B76252DD637F
P356
J.AJHG.2012.11.015
http://dx.doi.org/10.1016/J.AJHG.2012.11.015