Results 1 to 7 of 7
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TypeTitleAuthor(s)YearViews
Molecular characterization of haemophilia A in southern ChineseChan, V; Pang, A; Chan, TPT; Chan, VWY; Chan, TK1996123
 
Molecular characterization of haemophilia A in southern ChineseChan, VNY; Pang, A; Chan, TPT; Chan, VWY; Chan, TK199573
 
DNA analysis of Huntington's disease in Southern ChineseChan, V; Yu, YL; Chan, TPT; Yip, B; Chang, CM; Wong, MTH; Chan, YW; Chan, TK1995262
 
False non-paternity in a family for prenatal diagnosis of β-thalassaemiaChan, V; Chan, TPT; Lau, K; Todd, D; Chan, TK1993101
 
Molecular defects in haemophilia B: Detection by direct restriction enzyme analysisChan, V; Yip, B; Tong, TMF; Chan, TPT; Lau, K; Yam, I; Chan, TK199159
 
Multiple XbaI polymorphisms for carrier detection and prenatal diagnosis of haemophilia AChan, V; Tong, TMF; Chan, TPT; Tang, M; Wan, CW; Chan, FY; Chu, YC; Chan, TK198959
 
Restriction fragment length polymorphism in the interzeta hypervariable region for prenatal diagnosis of non-deletion α thalassemiaChan, V; Chan, TK; Wong, ACK; Chan, TPT; Ghosh, A; Todd, D198896
 
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