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Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype
  1. Correspondence to:
 Dr M Vekemans, Département de Génétique, Hôpital Necker-Enfants Malades, 149 rue de Sévres, 75015 Paris, France;
 vekemans{at}necker.fr
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Citation

Faivre L, Cormier-Daire V, Lapierre JM, et al
Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype

Publication history

  • First published August 1, 2002.
Online issue publication 
April 27, 2016

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