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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 11 April 2003
  • Accepted 3 June 2003
  • Published in print 1 February 2004.
  • Published online 2 February 2004.

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