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Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development
  1. Correspondence to:
 T Attié-Bitach
 Département de Génétique et Unité INSERM U-393, Hôpital Necker-Enfants Malades, 149, rue de Sèvres, 75743 Paris Cedex 15, France; tania.attie{at}necker.fr
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Sanlaville D, Etchevers HC, Gonzales M, et al
Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development

Publication history

  • Accepted August 18, 2005
  • Revised August 11, 2005
  • First published September 16, 2005.
Online issue publication 
March 08, 2006

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