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Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease
  1. Correspondence to:
 Stanislas Lyonnet
 Département de Génétique, Hôpital Necker-Enfants Malades, 149, rue de Sèvres, 75743 Paris Cedex 15, France; lyonnetnecker.fr
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Citation

Pelet A, de Pontual L, Clément-Ziza M, et al
Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease

Publication history

  • First published March 2, 2005.
Online issue publication 
April 27, 2016

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