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A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability
Cobben, J.M.; Weiss, M.M.; Dijk, F.S. van; Reuver, R. de; Kruiff, C. de; Pondaag, W.; ... ; Yntema, H.G. 2014
A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability
Article / Letter to editor
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