Showing results 1 to 6 of 6
| Title | Author(s) | Issue Date | |
|---|---|---|---|
Diagnostic value of whole‐exome sequencing in Chinese pediatric‐onset neuromuscular patients Journal:Molecular Genetics & Genomic Medicine | 2020 | ||
Monoallelic Mutations in CC2D1A Suggest a Novel Role in Human Heterotaxy and Ciliary Dysfunction Journal:Circulation: Genomic and Precision Medicine | 2020 | ||
Next generation sequencing in prenatal diagnosis Proceeding/Conference:American Society of Human Genetics Annual Meeting, ASHG2017 | 2017 | ||
Phenotypic and mutational spectrum of 21 Chinese patients with Alström syndrome Journal:American Journal of Medical Genetics Part A | 2020 | ||
Possible role(s) of interferon regulation of inflammasome activity via autophagy Proceeding/Conference:HKU Department of Paediatrics and Adolescent Medicine Golden Jubilee Scientific Meeting | 2014 | ||
Role of p53/p63 in chondrocyte re-differentiation upon activation of ER stress Proceeding/Conference:Research Postgraduate Symposium, RPS 2010 | 2010 |