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Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome.
Garavelli L, Donadio A, Zanacca C, Banchini G, Della Giustina E, Bertani G, Albertini G, Del Rossi C, Zweier C, Rauch A, Zollino M, Neri G. Garavelli L, et al. Among authors: zanacca c. Am J Med Genet A. 2003 Feb 1;116A(4):385-8. doi: 10.1002/ajmg.a.10855. Am J Med Genet A. 2003. PMID: 12522797 No abstract available.
[Home-coming diarrhea. Presentation of a clinical case].
de Angelis GL, Zanacca C, Banchini G, Caprio P, Bernasconi S. de Angelis GL, et al. Among authors: zanacca c. Pediatr Med Chir. 1987 Mar-Apr;9(2):237-8. Pediatr Med Chir. 1987. PMID: 3658808 Italian.
16 results