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Leukemia Research|August 4, 2004
Pathogenesis of jumping translocations: a molecular cytogenetics studyT S K Wan, S K Ma, E Y D Chow, et al.Cancer Genetics and Cytogenetics|September 1, 1994
Cytogenetics and immunophenotypes of childhood acute lymphoblastic leukemia in Hong KongL C Chan, S Y Ha, L M Ching, et al.Blood|November 15, 1994
Hereditary hemolytic anemia caused by diverse point mutations of pyruvate kinase gene found in Japan and Hong KongH Kanno, D C Wei, L C Chan, et al.Leukemia|August 5, 2006
The Mll-Een knockin fusion gene enhances proliferation of myeloid progenitors derived from mouse embryonic stem cells and causes myeloid leukaemia in chimeric miceC T Kong, M H Sham, C W E So, et al.American Journal of Hematology|May 1, 1995
Essential thrombocythemia: a retrospective analysis of 39 casesY L Kwong, R H Liang, E K Chiu, et al.The EMBO Journal|December 20, 1986
Rearrangement of immunoglobulin heavy chain genes in human T leukaemic cells shows preferential utilization of the D segment (DQ52) nearest to the J regionS Mizutani, A M Ford, L M Wiedemann, et al.British Journal of Haematology|August 6, 2000
Combination of stem cell factor and granulocyte colony-stimulating factor mobilizes the highest number of primitive haemopoietic progenitors as shown by pre-colony-forming unit (pre-CFU) assayM J Horsfall, C H Hui, L B To, et al.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.Pageof 19