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

@article{Garavelli2003HirschsprungDM,
  title={Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome.},
  author={Livia Garavelli and Anthony Donadio and Claudio Zanacca and Giacomo Banchini and Elvio Della Giustina and Gianna Bertani and Giuseppe Albertini and Carmine Del Rossi and Christiane Zweier and Anita Rauch and Marcella Zollino and Giovanni Neri},
  journal={American journal of medical genetics. Part A},
  year={2003},
  volume={116A 4},
  pages={385-8}
}