Congenital Arthrogryposis : An Extension of the 15q11.2 BP1-BP2 Microdeletion Syndrome?
Williams, C. A., Fairbrother, L. C., Usrey, K. M., Butler, Merlin G., Dasouki, Majed
Published in Case reports in genetics (01.01.2014)
Published in Case reports in genetics (01.01.2014)
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