Showing results 16 to 21 of 21
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| Title | Author(s) | Issue Date | Views | |
|---|---|---|---|---|
Rare variants in sporadic Hirschsprung disease patients Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2015 | 2015 | 60 | ||
A RET founder mutation in Chinese hirschsprung's patients Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009 | 2009 | 149 | ||
RET mutational spectrum in Hirschsprungs disease: evaluation of 601 Chinese patients Proceeding/Conference:International Congress of Human Genetics, ICHG 2011 | 2011 | 171 | ||
Whole exome sequencing analysis in biliary atresia: a follow-up study Proceeding/Conference:68th Annual Meeting of the American Society of Human Genetics, 2018 | 2018 | 51 | ||
Whole exome sequencing reveals a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia Proceeding/Conference:The 67th Annual Congress of the British Association of Paediatric Surgeons (Virtual), U.K. 7-9 July 2022 | 2021 | 11 | ||
Whole genome sequencing implicates rare variants in sporadic Hirschsprung disease Proceeding/Conference:European Human Genetics Conference (ESHG) 2017 | 2017 | 78 |