Showing results 2 to 8 of 8
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| Title | Author(s) | Issue Date | Views | |
|---|---|---|---|---|
Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS) Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012 | 2012 | 82 | ||
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 | 65 | ||
Functional characterisation reveals PTPN21 as a positive mediator of NRG3, a potential risk factor in Schizophrenia Proceeding/Conference:Research Postgraduate Symposium, RPS 2011 | 2011 | 122 | ||
Genetic study of a fami segregating Waardenburg-Shah syndrome Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012 | 2012 | 70 | ||
Genetic study of a family segregating Shah-Waardenburg syndrome Proceeding/Conference:ENS 2012 Meeting | 2012 | 67 | ||
Genome-wide copy number variation in anorectal malformations Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012 | 2012 | 90 | ||
Genomi-wide association study on anorectal malformations in the Chinese population Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010 | 2010 | 131 |