| Title | Author(s) | Year | View Count |
 | Molecular characterization of haemophilia A in southern Chinese | Chan, V; Pang, A; Chan, TPT; Chan, VWY; Chan, TK | 1996 | 154 |
 | Molecular characterization of haemophilia A in southern Chinese | Chan, VNY; Pang, A; Chan, TPT; Chan, VWY; Chan, TK | 1995 | 78 |
| DNA analysis of Huntington's disease in Southern Chinese | Chan, V; Yu, YL; Chan, TPT; Yip, B; Chang, CM; Wong, MTH; Chan, YW; Chan, TK | 1995 | 260 |
 | False non-paternity in a family for prenatal diagnosis of β-thalassaemia | Chan, V; Chan, TPT; Lau, K; Todd, D; Chan, TK | 1993 | 82 |
| Molecular defects in haemophilia B: Detection by direct restriction enzyme analysis | Chan, V; Yip, B; Tong, TMF; Chan, TPT; Lau, K; Yam, I; Chan, TK | 1991 | 45 |
| Multiple XbaI polymorphisms for carrier detection and prenatal diagnosis of haemophilia A | Chan, V; Tong, TMF; Chan, TPT; Tang, M; Wan, CW; Chan, FY; Chu, YC; Chan, TK | 1989 | 49 |
| Restriction fragment length polymorphism in the interzeta hypervariable region for prenatal diagnosis of non-deletion α thalassemia | Chan, V; Chan, TK; Wong, ACK; Chan, TPT; Ghosh, A; Todd, D | 1988 | 66 |
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