(Q85676342)
Statements
A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability (English)
J M Cobben
M M Weiss
F S van Dijk
R De Reuver
C de Kruiff
W Pondaag
R C Hennekam
30 September 2014