Showing results 1 to 3 of 3
Title | Author(s) | Issue Date | |
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Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease Proceeding/Conference:Neurogastroenterology and Motility | 2009 | ||
A RET founder mutation in Chinese hirschsprung's patients Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009 | 2009 | ||
RET mutational spectrum in Hirschsprungs disease: evaluation of 601 Chinese patients Proceeding/Conference:International Congress of Human Genetics, ICHG 2011 | 2011 |