Philadelphia chromosome unmasked as a secondary genetic change in acute myeloid leukemia on imatinib treatment von Yip, S F, Wan, T S K, Liu, H S Y, Wong, M L G, So, C-C, Chan, L C

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Characterization of additional genetic events in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion : a molecular cytogenetics study von MA, S. K, WAN, T. S. K, CHEUK, A. T. C, FUNG, L. F, CHAN, G. C. F, CHAN, S. Y, HA, S. Y, CHAN, L. C

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Derivative chromosome 9 deletions in chronic myeloid leukaemia: interpretation of atypical D-FISH pattern von Wan, T S K, Ma, S K, Au, W Y, Chan, L C

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Cytogenetics and molecular genetics of childhood leukemia von Ma, S. K., Wan, T. S. K., Chan, L. C.

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Fatal diffuse alveolar damage complicating acute myeloid leukemia with abnormal eosinophils and trisomy X von WAN, T. S. K, YIP, S. F, YEUNG, Y. M, CHAN, L. C, MA, S. K

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Prokineticin signaling is required for the maintenance of a de novo population of c-KIT super(+) cells to sustain neuroblastoma progression von Lau, S-T, Hansford, L M, Chan, W-K, Chan, G C-F, Wan, T S-K, Wong, K K-Y, Kaplan, D R, Tam, P K-H, Ngan, E S-W

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Amplification and overexpression of Aurora kinase A (AURKA) in immortalized human ovarian epithelial (HOSE) cells von Chung, C.M., Man, C., Jin, Y., Jin, C., Guan, X.Y., Wang, Q., Wan, T.S.K., Cheung, A.L.M., Tsao, S.W.

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Pathogenesis of jumping translocations: a molecular cytogenetics study von Wan, T.S.K, Ma, S.K, Chow, E.Y.D, Li, Y.H, Lin, S.Y, Chan, L.C

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Acquired pericentric inversion of chromosome 9 in essential thrombocythemia von Wan, T S, Ma, S K, Chan, L C

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Trisomy 21 and other chromosomal abnormalities in acute promyelocytic leukemia von Wan, T.S.K., Ma, S.K., Au, W.Y., Liu, H.S.Y., Chan, J.C.W., Chan, L.C.

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A dual colour dual fusion fluorescence in situ hybridisation study on the genesis of complex variant translocations in chronic myelogenous leukaemia von SO, Chi-Chiu, WAN, Thomas Shek-Kong, YIP, Sze-Fai, CHAN, Li-Chong

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Trisomy 21 as the sole acquired karyotypic abnormality in acute myeloid leukemia and myelodysplastic syndrome von Wan, T.S.K, Au, W.Y, Chan, J.C.W, Chan, L.C, Ma, S.K

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Two balanced and novel chromosomal translocations in myeloid malignancies: characterization by multiplex fluorescence in situ hybridization von Wan, T.S.K, Ma, S.K, Yip, S.F, Yeung, Y.M, Chan, L.C

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Presence of human papillomavirus in esophageal squamous cell carcinomas of Hong Kong Chinese and its relationship with p53 gene mutation von Lam, King-Yin, He, Dan, Ma, Lily, Zhang, Dekai, Ngan, Hextan Yuen-Sheung, Wan, Thomas Shek-Kong, Tsao, Sai-Wah

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Graft‐versus‐host disease after liver transplantation: documentation by fluorescent in situ hybridisation and human leucocyte antigen typing von Au, WY, Ma, SK, Kwong, YL, Ng, IOL, Hawkins, BR, Wan, TSK, Liu, CL, Fan, ST, Lo, CM

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Clonal Marrow Abnormalities after Azathioprine and Sulfasalazine Exposure in Crohn's Disease: A Cautionary Tale von Au, W.Y., Yuen, M.F., Lai, K.C., Wan, T.S.K., Ma, S.K.

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The role of trisomy 8 in the pathogenesis of chronic eosinophilic leukemia von Ma, S.K, Kwong, Y.L, Shek, T.W.H, Wan, T.S.K, Chow, E.Y.D, Chan, J.C.W, Chan, L.C

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Neutrophil functions of Chinese neonates von Wan, Tsk, Yeung, Cy, Tam, Ayc

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Quantum Mechanics: Problems and Solutions von Wan, K. Kong

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Establishment and Characterization of HKESC-1, a New Cancer Cell Line from Human Esophageal Squamous Cell Carcinoma von Hu, Ying-Chuan, Lam, King Y, Wan, Thomas S.K, Fang, Wei-Gang, Ma, Edmond S.K, Chan, Li C, Srivastava, Gopesh

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