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Mowat–Wilson syndrome and mutation in the zinc finger homeo box 1B gene: a well defined clinical entity
  1. Correspondence to:
 Dr P Cerruti Mainardi
 Divisione di Pediatria – Servizio di Genetica, Ospedale S. Andrea, Corso Abbiate 21, 13100 Vercelli, Italy; pcerrutinet4u.it
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Cerruti Mainardi P, Pastore G, Zweier C, et al
Mowat–Wilson syndrome and mutation in the zinc finger homeo box 1B gene: a well defined clinical entity

Publication history

  • Received April 11, 2003
  • Accepted June 3, 2003
  • First published February 2, 2004.

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