(Q51951191)
Statements
Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome (English)
L Garavelli
A Donadio
C Zanacca
G Banchini
E Della Giustina
G Bertani
G Albertini
C Del Rossi
A Rauch
M Zollino
1 February 2003