Showing results 16 to 21 of 21
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| Title | Author(s) | Issue Date | |
|---|---|---|---|
Fine mapping on chromosome 10q24.2 implicates ADD3 in biliary atresia Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012 | 2012 | ||
Fine mapping of the NRG1 Hirschsprung's-associated gene Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010 | 2010 | ||
Fine mapping of Hirschsprung’s disease loci in 9q31 Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009 | 2009 | ||
Exome sequencing reveals a recessive mechanism involving interacting genes in persistent cloaca Proceeding/Conference:Annual International Congress of the British Association of Paediatric Surgeons, BAPS 2016 | 2016 | ||
Deciphering the genetic basis of Hirschsprung disease by whole genome sequencing Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2016 | 2016 | ||
ATP-binding cassette (ABC) transporter recessive mutations in biliary atresia cases Proceeding/Conference:American Society of Human Genetics (ASHG) 2019 Annual Meeting | 2019 |