We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMutations of the RET gene in isolated and syndromic Hirschsprung’s disease in human disclose major and modifier alleles at a single locusAuthorsde Pontual, L; Pelet, A; Trochet, D; Jaubert, F; Espinosa-Parrilla, Y; Munnich, A; Brunet, J-F; Goridis, C; Feingold, J; Lyonnet, S; Amiel, JPublicationJournal of Medical Genetics (JMG), 2006, Vol 43, Issue 5, p419ISSN0022-2593Publication typearticle