Browsing by Author Lee, SL

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TitleAuthor(s)Issue DateViews
 
Editor(s):Limdi, N
2021
14
 
Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population (e-poster)
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
47
 
2021
50
 
Actionable secondary findings in Hong Kong Chinese based on exome sequencing data
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
4
 
2014
77
 
Airway abnormalities in Congenital Heart Disease in Children - Review of Local Experience
Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)
1997
23
 
2002
91
 
An Efficient Cardiac Mapping Strategy for Radiofrequency Catheter Ablation with Active Learning
Journal:International Journal of Computer Assisted Radiology and Surgery
2017
13
 
Anti-NMDA-R encephalitis: an encephalitis lerthargica-like illness
Proceeding/Conference:Hong Kong Medical Journal
2009
136
 
Anti-NMDAR encephalitis: An encephalitis lethargica like illness
Proceeding/Conference:International Child Neurology Congress (ICNC)
2010
2012
59
 
2006
179
 
2004
 
Asthma Readmission Rates of Hong Kong Children
Proceeding/Conference:Guangdong-Hong Kong 2004 Paediatrics Exchange Meeting
2004
105
 
Asthma Readmission Rates of Hong Kong Children
Proceeding/Conference:Hong Kong Journal of Paediatrics
2004
 
1-Jul-2023
 
2019
122
 
2017
110
 
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
87
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
2014