Browsing by Author Yeung, KS

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing results 64 to 77 of 77 < previous 
TitleAuthor(s)Issue DateViews
 
Rare SUZ12 variants commonly cause an overgrowth phenotype
Journal:American Journal of Medical Genetics Part C: Seminars in Medical Genetics
2019
22
 
Reading NGS Test Report: What a clinician needs to know
Proceeding/Conference:HA 2016 Commissioned Training Programme - Genetics in O&G
2016
19
 
Retrospective cohort analysis on couples seeking pre-implantation genetic testing over a 5-year period
Proceeding/Conference:Joint Annual Scientific Meeting 2020 of The Hong Kong Paediatric Society (HKPS), Hong Kong College of Paediatricians (HKCPaed), Hong Kong Paediatric Nurses Association (HKPNA) and Hong Kong College of Paediatric Nursing (HKCPN)
2020
22
 
Silver-Russell syndrome in Hong Kong
Journal:Hong Kong Medical Journal
2016
60
 
Somatic mosaicism of PIK3CA mutation in PIK3CA-related overgrowth disorders
Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2014
2014
72
 
2017
68
 
2014
75
 
2008
80
 
2016
44
 
1992
60
 
2017
160
 
2020
46
 
The KLHL40C.1516A>C is a Chinese-specific founder mutation in causing nemaline myopathy 8
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
31
 
1993
69