(Q51909612)
Statements
A homozygous deletion of 8q24.3 including the NIBP gene associated with severe developmental delay, dysgenesis of the corpus callosum, and dysmorphic facial features. (English)
1 reference
Arie Koifman
1 reference
Annette Feigenbaum
1 reference
Weimin Bi
1 reference
Lisa G Shaffer
1 reference
Jill Rosenfeld
1 reference
Susan Blaser
1 reference
David Chitayat
1 reference
1 May 2010
1 reference
152A
1 reference
5
1 reference
1268-1272
1 reference