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Comment
. 2003 Feb 1;116A(4):385-8.
doi: 10.1002/ajmg.a.10855.

Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome

L Garavelli, A Donadio, C Zanacca, G Banchini, E Della Giustina, G Bertani, G Albertini, C Del Rossi, C Zweier, A Rauch, M Zollino, G Neri
Comment

Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome

L Garavelli et al. Am J Med Genet A. .
No abstract available

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