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J.EJMG.2011.05.004
J.EJMG.2011.05.004
http://dx.doi.org/10.1016/J.EJMG.2011.05.004
A de novo 1.1Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformation.
P356
Q37893763-689CBF6B-C525-4F89-B340-B7F0863B39F7
P356
J.EJMG.2011.05.004
http://dx.doi.org/10.1016/J.EJMG.2011.05.004