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In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome
  1. Correspondence to:
 Dr V Cormier-Daire, Département de Génétique, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France; 
 cormier{at}necker.fr
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Citation

Faivre L, Gorlin RJ, Wirtz MK, et al
In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome

Publication history

  • Accepted September 18, 2002
  • Revised September 17, 2002
  • First published January 1, 2003.
Online issue publication 
April 27, 2016

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