| Type | Title | Author(s) | Year | Views |
| No NRG1 V266L in Chinese patients with schizophrenia | GarciaBarceló, MM; Miao, X; Tang, CS; So, HC; Tang, W; Leon, TYY; So, M; Yip, B; Chen, RYL; Cheung, EFC; Chen, EYH; Li, T; Tam, P; Cherny, SS; Sham, PC | 2011 | 423 |
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| Gray matter in first-episode schizophrenia before and after antipsychotic drug treatment. Anatomical likelihood estimation meta-analyses with sample size weighting | Leung, M; Cheung, C; Yu, K; Yip, B; Sham, P; Li, Q; Chua, S; McAlonan, G | 2011 | 307 |
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| Evaluation of a psychoeducation program for Chinese clients with schizophrenia and their family caregivers | Chan, SWC; Yip, B; Tso, S; Cheng, Bs; Tam, W | 2009 | 106 |
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| Carrier incidence for spinal muscular atrophy in southern Chinese | Chan, V; Yip, B; Yam, I; Au, P; Lin, CK; Wong, V; Chan, TK | 2004 | 107 |
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| A new cross-over region for hemogloboin-Lepore-Hollandia | Chan, V; Au, P; Yip, B; Chan, TK | 2004 | 53 |
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| A genetic locus for adolescent idiopathic scoliosis linked to chromosome 19p13.3 | Chan, V; Fong, GCY; Luk, KDK; Yip, B; Lee, MK; Wong, MS; Lu, DDS; Chan, TK | 2002 | 264 |
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| Quantitative polmerase chain reaction for the rapid prenatal diagnosis of homozygous α-thalassaemia (HB Barts hydrops fetalis) | Chan, V; Yip, B; Lam, YH; Tse, HY; Wong, HS; Chan, TK | 2001 | 64 |
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| Novel type of BCR-ABL transcript in a chronic myelogenous leukaemia patient relapsed after bone marrow transplantation | Chan, V; Yam, I; Yip, B; Au, P; Shing, MK; Li, CK; Chan, TK | 2000 | 63 |
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| Hemophilia B in a female carrier due to skewed inactivation of the normal X-chromosome | Chan, V; Chan, VWY; Yip, B; Chim, CS; Chan, TK | 1998 | 79 |
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| Diagnosis of spinal muscular atrophy from fetal normoblasts in maternal blood | Chan, V; Lau, K; Yip, B; Sin, SY; Cheung, MC; Kan, YW | 1998 | 55 |
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| A semi-automated method for analysis of intron 13 and intron 22 dinucleotide repeat polymorphisms of the factor VIII gene | Yip, B; Chan, V; Chan, TK | 1996 | 90 |
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| A semi-automated allele specific PCR for detection of beta thalassemia mutations | Chan, VNY; Yip, B; Lau, K; Chan, TK | 1996 | 65 |
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| A semi-automated method for analysis of microsatellite repeat polymorphisms in the factor VIII gene (Abstract) | Yip, B; Chan, VNY; Chan, TK | 1995 | 72 |
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| 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 | 256 |
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| A semi-automated method for analysis of microsatellite repeat polymorphisms in the factor VIII gene | Yip, B; Chan, VNY; Chan, TK | 1995 | 66 |
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| Uses of dinucleotide/trinucleotide repeats in the diagnosis of genetic diseases. | Chan, V; Yip, B; Chan, TP; Chan, TK | 1995 | 47 |
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| Intragenic dinucleotide repeats in factor VIII gene for the diagnosis of haemophilia A | Yip, B; Chan, V; Chan, TK | 1994 | 62 |
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| 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 | 56 |
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