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Mutations of the RET gene in isolated and syndromic Hirschsprung’s disease in human disclose major and modifier alleles at a single locus
  1. Correspondence to:
 Dr Jeanne Amiel
 Département de Génétique, Hôpital Necker-Enfants Malades, 149, rue de Sèvres, 75743 Paris Cedex 15, France; amiel{at}necker.fr
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Citation

de Pontual L, Pelet A, Trochet D, et al
Mutations of the RET gene in isolated and syndromic Hirschsprung’s disease in human disclose major and modifier alleles at a single locus

Publication history

  • Received December 7, 2005
  • Accepted January 19, 2006
  • Revised January 2, 2006
  • First published January 27, 2006.
Online issue publication 
April 28, 2006

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