Browsing by Author Chan, YW

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TitleAuthor(s)Issue DateViews
 
Molecular characterization of the 2011 Hong Kong scarlet fever outbreak
Journal:Journal of Infectious Diseases
Tse, HBao, JYJDavies, MRMaamary, PTsoi, HWTong, AHYHo, TCCLin, CHGillen, CMBarnett, TCChen, JHKLee, MYam, WCWong, CKOng, CLYChan, YWWu, CWNg, TLim, WWLTsang, THFTse, CWSDougan, GWalker, MJLok, SYuen, KY
2012
200
 
Molecular Identification and Characterization of The Hog Cholera Virus From Hong Kong and South China
Proceeding/Conference:International Symposium of Society of Chinese Bioscientists in America
Wong, KMWu, HChan, YWLeung, FCC
1999
89
 
Molecular Identification of Hog Cholera Viruses from Southern China
Journal:Journal of Animal and Veterinary Advances
Wu, HZChan, YWWong, KMLeung, FCC
2005
89
 
Motor neuron disease in Hong Kong Chinese: Epidemiology and clinical picture
Journal:Neuroepidemiology
Fong, KYYu, YLChan, YWKay, RChan, JYang, ZKwan, MCLeung, KPLi, PCKLam, THCheung, RTF
1996
143
 
Motor Neurone Disease (MND) in Hong Kong Chinese: Neuroepidemiology and Clinical Features
Proceeding/Conference:1st Asian-Oceanian Symposium in neuroepidemiology & 2nd Wu Ho-Su Memorial Lecture
Fong, KYYu, YLChan, YWLeung, KPLi, PCKLam, THYang, ZKwan, MCKay, RChan, JCheung, RTF
1994
121
 
Mouse models of atherosclerosis: a historical perspective and recent advances
Journal:Lipids in Health and Disease
Lee, YTLin, HYChan, YWLi, KHTo, OTYan, BPLiu, TLi, GPWong, WTKeung, WWYTse, G
2017
94
 
MSH2 c.1452-1455delAATG Is a Founder Mutation and an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Southern Chinese Population
Journal:American Journal of Human Genetics
Chan, TLChan, YWHo, JWCChan, CChan, ASYChan, ELam, PWYTse, CWLee, KCLau, CWGwi, ELeung, SYYuen, ST
2004
122
 
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity
Journal:Journal of Human Genetics
Mak, CMLam, CWTam, SLai, CLChan, LYFan, STLau, YLLai, JYYuen, PHui, JFu, CCWong, KSMak, WLTze, KTong, SFLau, ALeung, NHui, ACheung, KMKo, CHChan, YKMa, OChau, TNChiu, AChan, YW
2008
172
 
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity (Journal of Human Genetics (2008) 53 (55-63) DOI: 10.1007/s10038-007-0218-2)
Journal:Journal of Human Genetics
Mak, CMLam, CWTam, SLai, CLChan, LYFan, STLau, YLLai, STYuen, PHui, JFu, CCWong, KSMak, WLTze, KTong, SFLau, ALeung, NHui, ACheung, KMKo, CHChan, YKMa, OChau, TNChiu, AChan, YW
2008
184
 
Non-invasive screening of HLA-DPA1 and HLA-DPB1 alleles for persistent hepatitis B virus infection: Susceptibility for vertical transmission and toward a personalized approach for vaccination and treatment
Journal:Clinica Chimica Acta
Lau, KCLam, CWLaw, CYLai, STTsang, TYSiu, CWKTo, WKLeung, KFMak, CMPoon, WTChan, PKSChan, YW
2011
133
 
Novel donor splice site mutation of ABCG5 gene in sitosterolemia
Journal:Molecular Genetics and Metabolism
Lam, CWCheng, AWFTong, SFChan, YW
2002
173
 
A novel missense mutation (P191L) in the glucose-6-phosphate translocase gene identified in a Chinese family with glycogen storage disease 1b.
Journal:Human mutation
Lam, CWChan, KYTong, SFChan, BYChan, YTChan, YW
2000
111
 
Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b
Journal:Molecular Genetics and Metabolism
Yuen, YPCheng, WFTong, SFChan, YTChan, YWLam, CW
2002
166
 
Novel missense mutation (Y279S) in the GLRA1 gene causing hyperekplexia [2]
Journal:Clinica Chimica Acta
Poon, WTAu, KMChan, YWChan, KYChow, CBTong, SFLam, CW
2006
170
 
Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC
Journal:Clinical Chemistry
Lam, CWPoon, PMKTong, SFLo, AWILai, CKChoi, KLTiu, SCChan, YWShek, CC
2001
98
 
Novel mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donor
Journal:American Journal of Kidney Diseases
Lam, CWYuen, YPLai, CKTong, SFLau, LKTong, KLChan, YW
2001
149
 
A novel mutation, Y255X, of the ARSB gene in a Chinese family with mucopolysaccharidosis type VI
Journal:Chinese Medical Journal
Lam, CWChan, AOKLai, CKChan, WHChan, YWShek, CCTong, SF
2004
126
 
Novel mutations in the BCHE gene in patients with no butyrylcholinesterase activity
Journal:Clinica Chimica Acta
OnKei Chan, ALam, CWTong, SFMan Tung, CYung, KChan, YWAu, KMYuen, YPHung, CTNg, KPShek, CC
2005
125
 
Novel mutations of the AGXT gene causing primary hyperoxaluria type 1
Journal:Journal of Nephrology
Yuen, YPLai, CKTong, GMWWong, PNWong, FKMMak, SKLo, KYWong, AKMTong, SFChan, YWLam, CW
2004
126
 
Novel splicing mutation of the PPOX gene (IVS10+1G→A) detected by denaturing high-performance liquid chromatography
Journal:Clinica Chimica Acta
Lam, CWHui, KNPoon, PMKLuk, NMYuen, YPTong, SFLai, CKChan, YWLo, KK
2001
176
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