Showing results 1 to 8 of 8
| Title | Author(s) | Issue Date | |
|---|---|---|---|
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 | ||
Genome-wide copy number variation in anorectal malformations Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012 | 2012 | ||
Genetic study of a family segregating Shah-Waardenburg syndrome Proceeding/Conference:ENS 2012 Meeting | 2012 | ||
Genetic study of a fami segregating Waardenburg-Shah syndrome Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012 | 2012 | ||
Functional characterisation reveals PTPN21 as a positive mediator of NRG3, a potential risk factor in Schizophrenia Proceeding/Conference:Research Postgraduate Symposium, RPS 2011 | 2011 | ||
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 | ||
Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS) Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012 | 2012 | ||
Comprehensive comparison of copy number variations detection using Illumina Omni 2.5M and Affymetrix CytoScan® arrays Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013 | 2013 |