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

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)385-388
Number of pages4
JournalAmerican Journal of Medical Genetics
Volume116 A
Issue number4
Publication statusPublished - Feb 1 2003

ASJC Scopus subject areas

  • Genetics(clinical)

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