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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
- 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
Citation
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 27, 2016
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Copyright 2006 Journal of Medical Genetics