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NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome
  1. Correspondence to:
 Valérie Cormier-Daire
 INSERM U393, Hôpital Necker - Enfants Malades, 149 Rue de Sèvres, 75015 Paris, France; cormiernecker.fr
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Citation

Borck G, Redon R, Sanlaville D, et al
NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome

Publication history

  • Accepted September 23, 2004
  • Revised September 21, 2004
  • First published December 9, 2004.
Online issue publication 
April 27, 2016

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