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Human Pathology|July 22, 1999
The role of trisomy 8 in the pathogenesis of chronic eosinophilic leukemiaS K Ma, Y L Kwong, T W Shek, et al.International Journal of Molecular Medicine|January 20, 2000
Absence of microsatellite instability in primary myelodysplastic syndromeS K Ma, C T Kong, T S Wan, et al.American Journal of Hematology|June 22, 2000
beta-thalassemia intermedia caused by compound heterozygosity for Hb Malay (beta codon 19 AAC-->AGC; asn-->Ser) and codons 41/42 (-CTTT) beta(0)-thalassemia mutationS K Ma, E Y Chow, A Y Chan, et al.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.Pageof 93