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Journal of Clinical Pathology|April 18, 2001
Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?L C Chan, S K Ma, A Y Chan, et al.Cancer Genetics and Cytogenetics|February 1, 1994
Inversion (14)(q11q32) in childhood T-cell acute lymphoblastic leukemiaY L Kwong, M K Shing, T M Wan, et al.Cancer Genetics and Cytogenetics|March 21, 2003
Trisomy 21 and other chromosomal abnormalities in acute promyelocytic leukemiaT S K Wan, S K Ma, W Y Au, et al.Leukemia|January 1, 1994
Clonal expansion of p53 mutant cells in leukemia progression in vitroH Wada, M Asada, S Nakazawa, et al.The New England Journal of Medicine|May 1, 1997
Prevalence and genotypes of alpha- and beta-thalassemia carriers in Hong Kong -- implications for population screeningY L Lau, L C Chan, Y Y Chan, et al.Leukemia|November 22, 1997
The spectrum of chronic lymphoproliferative disorders in Hong Kong. A prospective studyL C Chan, C K Lam, T C Yeung, et al.Clinical and Laboratory Haematology|June 26, 2001
Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese familyK F Leung, W Y Au, A Y Chan, et al.British Journal of Haematology|December 19, 1998
Near-haploid common acute lymphoblastic leukaemia of childhood with a second hyperdiploid line: a DNA ploidy and fluorescence in-situ hybridization studyS K Ma, G C Chan, T S Wan, et al.Journal of Medical Genetics|August 14, 2008
The HBS1L-MYB intergenic region on chromosome 6q23 is a quantitative trait locus controlling fetal haemoglobin level in carriers of beta-thalassaemiaC-C So, Y-Q Song, S T Tsang, et al.American Journal of Clinical Pathology|January 1, 1995
Large granular lymphocyte leukemia. A study of nine cases in a Chinese populationY L Kwong, K F Wong, L C Chan, et al.Pageof 19