(Q79619487)
Statements
Contiguous gene syndrome due to a maternally inherited 8.41 Mb distal deletion of chromosome band Xp22.3 in a boy with short stature, ichthyosis, epilepsy, mental retardation, cerebral cortical heterotopias and Dandy-Walker malformation (English)
M Vreeburg
J Engelen
S Ghesquiere
A P A Stegmann
J Herbergs
J van Lent
B Smeets
1 November 2008