Browsing "Obstetrics & Gynaecology: Conference papers" by Author lee, sl

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TitleAuthor(s)Issue Date
 
CFTR: p.I1023R is a rare but recurrent disease-causing mutation found in Chinese patients with Cystic Fibrosis
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2014
Chung, BHYLeung, KCMak, CCYChow, CSKYing, JDChu, YWYYang, WLLau, YLChan, KYKLee, SL
2014
 
Copy number variation in Hong Kong patients with autism spectrum disorder
Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)
Mak, ASLLeung, GKCMak, CCYChu, YWYMok, GTKTang, TWFChan, KYKKan, ASYTang, MHYLau, ETKSo, KWTao, QVFung, CWWong, VCNLee, SLChung, BHY
2016
 
Identification of a CFTR founder mutations, c.3068T>G:p.I1023R, which causes protein trafficking defects in Chinese patients with cystic fibrosis
Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016
Leung, KCYing, DMak, CCYChen, XYXu, WYeung, KSChu, WYMok, TKGChau, SKCMcLuskey, JOng, WPTLeong, HYChan, YKYang, WChen, JHLi, AMLau, YLLee, SLChung, BHY
2016
 
Use of chromosomal microarray in Hong Kong patients with autism spectrum disorder - implication of a copy number variation involving DPP10
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2016
Chung, BHYMak, SLChiu, TALeung, KCMak, CCYChu, WYMok, TKGChan, YKKan, SYATang, MHYLau, ETKFung, CWLee, SL
2016
 
Use of clinical chromosomal microarray in Hong Kong Chinese patients with autism spectrum disorder - implication of a copy number variation involving DPP10
Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016
Chu, YWYLeung, KCMak, ASLChiu, TAMak, CCYMok, TKGTang, WFChan, YKTang, MHYLau, ETKSo, KWTao, QVFung, CWWong, VCNLee, SLMarshall, CScherer, SKan, SYAChung, BHY
2016
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