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Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females
  1. Correspondence to Dr C Philippe, Laboratoire de Génétique Médicale, Nancy Université, EA 4002, Centre Hospitalier Régional et Universitaire, Rue du Morvan, 54511 cedex 1, Vandoeuvre-les-Nancy, France; c.philippe{at}chu-nancy.fr
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Citation

Philippe C, Amsallem D, Francannet C, et al
Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females

Publication history

  • Received February 24, 2009
  • Revised April 20, 2009
  • Accepted April 29, 2009
  • First published June 29, 2009.
Online issue publication 
January 11, 2010

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