Showing results 1 to 10 of 10
| Title | Author(s) | Issue Date | |
|---|---|---|---|
Clinical utility of whole-genome sequencing for cytogenetically balanced chromosomal abnormalities in genetic diseases Proceeding/Conference:Joint Annual Scientific Meeting 2019 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association, &
Hong Kong College of Paediatric Nursing | 2019 | ||
| 2022 | |||
| 2012 | |||
Epigenetic dysregulation in hepatocellular carcinoma: focus on polycomb group proteins Journal:Frontiers of Medicine | 2013 | ||
Exome sequencing identifies compound heterozygous DYNC2H1 variants associated with short-rib polydactyly syndrome type III with involvement of omphalocele in a fetus. Proceeding/Conference:23rd Internatinal Conference on Prenatal Diagnosis and Therapy (ISPD 2019) | 2019 | ||
| 2013 | |||
| 2013 | |||
| 2017 | |||
| 2014 | |||
| 2015 |