Showing results 1 to 7 of 7
| Title | Author(s) | Issue Date | |
|---|---|---|---|
CFTR: I1023R is a rare but recurrent disease-causing mutation found in Chinese patients with cystic fibrosis Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2014 | 2014 | ||
Challenges faced by little people of Hong Kong: narrative medicine in clinical genetics practice Proceeding/Conference:HKU Department of Paediatrics & Adolescent Medicine Golden Jubilee Scientific Meeting | 2014 | ||
Computer-aided facial recognition of Chinese individuals with Angelman syndrome in Hong Kong Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians cum Hong Kong-Guangdong-Shanghai-Chongqing Paediatric Exchange Meeting, 2016 | 2016 | ||
Identification of epigenetic alterations in imprinting growth disorders Proceeding/Conference:HKU Department of Paediatrics & Adolescent Medicine Golden Jubilee Scientific Meeting | 2014 | ||
Inheritance and risk assessment Proceeding/Conference:HA 2014 Commissioned Program: Clinical Genetics & Genetic Counseling for nurses - Clinical Genetics in Paediatrics | 2014 | ||
Paediatric counseling & scenarios Proceeding/Conference:HA 2014 Commissioned Program: Clinical Genetics & Genetic Counseling for nurses - Clinical Genetics in Paediatrics | 2014 | ||
The genetics of macrocephaly, autistic spectrum disorders and developmental delay in Chinese children Proceeding/Conference:Developmental Medicine and Child Neurology | 2017 |