Results 1 to 20 of 58
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TypeTitleAuthor(s)YearViews
Molecular characterization of the 2011 Hong Kong scarlet fever outbreakTse, H; Bao, JYJ; Davies, MR; Maamary, P; Tsoi, HW; Tong, AHY; Ho, TCC; Lin, CH; Gillen, CM; Barnett, TC; Chen, JHK; Lee, M; Yam, WC; Wong, CK; Ong, CLY; Chan, YW; Wu, CW; Ng, T; Lim, WWL; Tsang, THF; Tse, CWS; Dougan, G; Walker, MJ; Lok, S; Yuen, KY2012124
 
Circulating fluorocytes at the first attack of acute intermittent porphyria: A missing link in the pathogenesisLam, CW; Lau, KC; Mak, CM; Tsang, MW; Chan, YW2011191
 
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 treatmentLau, KC; Lam, CW; Law, CY; Lai, ST; Tsang, TY; Siu, CWK; To, WK; Leung, KF; Mak, CM; Poon, WT; Chan, PKS; Chan, YW2011204
 
Young-onset Parkinsonism in a Hong Kong Chinese man with adult-onset Hallervorden-Spatz syndromeMak, CM; Sheng, B; Lee, HHC; Lau, KK; Chan, WT; Lam, CW; Chan, YW2011168
 
Maternally inherited leigh syndrome: An unusual cause of infantile apneaChau, CSK; Kwok, KL; Ng, DK; Lam, CW; Tong, SF; Chan, YW; Siu, WK; Yuen, YP2010210
 
Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong ChineseMak, CM; Lam, CW; Siu, TS; Chan, KY; Siu, WK; Yeung, WL; Hui, J; Wong, VCN; Low, LCK; Ko, CH; Fung, CW; Chen, SP; Yuen, YP; Lee, HC; Yau, E; Chan, B; Tong, SF; Tam, S; Chan, YW2010239
 
Pectoralis major flapWei, WI; Chan, YW2009153
 
Prospective randomized study of selective neck dissection versus observation for N0 neck of early tongue carcinomaYuen, PW; Ho, CM; Chow, TL; Tang, LC; Cheung, WY; Ng, WM; Wei, WI; Kong, CK; Book, KS; Yuen, WC; Lam, AK; Yuen, NW; Trendell-Smith, NJ; Chan, YW; Wong, BYH; Li, GKH; Ho, ACW; Ho, WK; Wong, SY; Yao, TJ2009392
 
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)Mak, CM; Lam, CW; Tam, S; Lai, CL; Chan, LY; Fan, ST; Lau, YL; Lai, ST; Yuen, P; Hui, J; Fu, CC; Wong, KS; Mak, WL; Tze, K; Tong, SF; Lau, A; Leung, N; Hui, A; Cheung, KM; Ko, CH; Chan, YK; Ma, O; Chau, TN; Chiu, A; Chan, YW2008153
 
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneityMak, CM; Lam, CW; Tam, S; Lai, CL; Chan, LY; Fan, ST; Lau, YL; Lai, JY; Yuen, P; Hui, J; Fu, CC; Wong, KS; Mak, WL; Tze, K; Tong, SF; Lau, A; Leung, N; Hui, A; Cheung, KM; Ko, CH; Chan, YK; Ma, O; Chau, TN; Chiu, A; Chan, YW2008226
 
Germline epimutation of MLH1 in early-onset colorectal cancerChan, TL; Tsui, WY; Chan, YW; Chan, ASY; Lee, TYH; Yuen, ST; Leung, SY2008203
 
Study of the mechanisms underlying heritable germline epimutation of MSH2 in a Hereditary Nonpolyposis Colorectal Cancer familyChan, TL; Yuen, ST; Lo, MWS; Lee, TYH; Kong, CK; Chan, YW; Tsui, WY; Li, VSW; Chan, ASY; Leung, SY2007190
 
Immunohistochemical staining on tissue microarray of colorectal cancers constitutes a convenient means to rapidly screen for MMR deficiencyChan, TL; Guo, D; Yuen, ST; Chan, YW; Chan, ASY; Leung, SY2007174
 
DNA-based diagnosis of methylmalonic aciduria and homocystinuria, cblC type in a Chinese patient presenting with mild developmental delayYuen, YP; Lam, CW; Chan, KY; Lai, CK; Tong, SF; Chan, YW200768
 
Heritable germline epimutation of MSH2 in a hereditary nonpolyposis colorectal cancer familyChan, TL; Yuen, ST; Kong, CK; Chan, YW; Chan, ASY; Leung, SY2007202
 
Microsatellite instability and novel mismatch repair gene mutations in northern Chinese population with hereditary non-polyposis colorectal cancer.Sheng, JQ; Chan, TL; Chan, YW; Huang, JS; Chen, JG; Zhang, MZ; Guo, XL; Mu, H; Chan, AS; Li, SR; Yuen, ST; Leung, SY2006177
 
Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuriaYuen, YP; Lam, CW; Lai, CK; Tong, SF; Li, PS; Tam, S; Kwan, EYW; Chan, SY; Tsang, WK; Chan, KY; Mak, WL; Cheng, CW; Chan, YW2006106
 
Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancerChan, TL; Yuen, ST; Kong, CK; Chan, YW; Chan, ASY; Ng, WF; Tsui, WY; Lo, MWS; Tam, WY; Li, VSW; Leung, SY2006143
 
Novel missense mutation (Y279S) in the GLRA1 gene causing hyperekplexia [2]Poon, WT; Au, KM; Chan, YW; Chan, KY; Chow, CB; Tong, SF; Lam, CW200663
 
Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndromeLam, CW; Yuen, YP; Cheng, WF; Chan, YW; Tong, SF200685
 
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