A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability

Author(s):
Cobben, J.M.; Weiss, M.M.; Dijk, F.S. van; Reuver, R. de; Kruiff, C. de; Pondaag, W.; Hennekam, R.C.; Yntema, H.G.
Published
2014
Publication type
Article / Letter to editor
ZMYND11ExomeSyndromic ID10p15.3
Date issued
2014-12-31
Language
English
Is part of
European Journal of Medical Genetics (2014), Vol. 57, no. 11-12, p. 636-638
hdl
1887/105359
doi
10.1016/j.ejmg.2014.09.002