Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): Confirmation of the Mowat-Wilson syndrome [1]

Livia 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

Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): Confirmation of the Mowat-Wilson syndrome [1]

Livia 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

Arcispedale Santa Maria Nuova

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	385-388
Number of pages	4
Journal	American Journal of Medical Genetics
Volume	116 A
Issue number	4
Publication status	Published - Feb 1 2003

ASJC Scopus subject areas

Genetics(clinical)

Cite this

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. (2003). Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): Confirmation of the Mowat-Wilson syndrome [1]. American Journal of Medical Genetics, 116 A(4), 385-388.

Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1) : Confirmation of the Mowat-Wilson syndrome [1]. / Garavelli, Livia; Donadio, A.; Zanacca, C.; Banchini, G.; Della Giustina, E.; Bertani, G.; Albertini, G.; Del Rossi, C.; Zweier, C.; Rauch, A.; Zollino, M.; Neri, G.

In: American Journal of Medical Genetics, Vol. 116 A, No. 4, 01.02.2003, p. 385-388.

Research output: Contribution to journal › Article › peer-review

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 2003, 'Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): Confirmation of the Mowat-Wilson syndrome [1]', American Journal of Medical Genetics, vol. 116 A, no. 4, pp. 385-388.

Garavelli, Livia ; Donadio, A. ; Zanacca, C. ; Banchini, G. ; Della Giustina, E. ; Bertani, G. ; Albertini, G. ; Del Rossi, C. ; Zweier, C. ; Rauch, A. ; Zollino, M. ; Neri, G. / Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1) : Confirmation of the Mowat-Wilson syndrome [1]. In: American Journal of Medical Genetics. 2003 ; Vol. 116 A, No. 4. pp. 385-388.

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