1. Mutations of the RET gene in isolated and syndromic Hirschsprung's disease in human disclose major and modifier alleles at a single locus. Issue 5 (27th January 2006) Authors: de Pontual, L; Pelet, A; Trochet, D; Jaubert, F; Espinosa-Parrilla, Y; Munnich, A; Brunet, J-F; Goridis, C; Feingold, J; Lyonnet, S; Amiel, J Journal: Journal of medical genetics Issue: Volume 43:Issue 5(2006) Page Start: 419 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗