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A E Watmore

Showing results (1-10 of 16) with videos related to

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Cancer Genetics and Cytogenetics|March 25, 2000
Acute monocytic leukemia with a novel 10;11 rearrangement resolved by fluorescence in situ hybridizationE J Sinclair, S Jalihal, A E Watmore
Cancer Genetics and Cytogenetics|April 15, 1985
Nonendemic Burkitt's lymphoma with complex chromosome abnormalities involving chromosomes 2 and 8A E Watmore, J A Murray, A M Potter
Cancer Genetics and Cytogenetics|January 15, 1985
Value of cytogenetic studies in prediction of acute phase CMLA E Watmore, A M Potter, R J Sokol, et al.
Cancer Genetics and Cytogenetics|July 15, 1988
Methotrexate and bone marrow metaphasesJ J Cunningham, A M Potter, A E Watmore, et al.
Journal of Clinical Pathology|January 1, 1991
Chromosomes in childhood acute lymphoblastic leukaemia: karyotypic patterns in disease subtypesM A Wodzinski, A E Watmore, J S Lilleyman, et al.
Cancer Genetics and Cytogenetics|August 5, 1998
Trisomy 15 associated with loss of the Y chromosome in bone marrow: a possible new aging effectE J Sinclair, A M Potter, A E Watmore, et al.
British Journal of Cancer|July 1, 1981
Significance of non-standard Philadelphia chromosomes in chronic granulocytic leukaemiaA M Potter, A E Watmore, P Cooke, et al.
Cancer Genetics and Cytogenetics|August 25, 1999
Consistent fusion of MOZ and TIF2 in AML with inv(8)(p11q13)M Carapeti, R C Aguiar, A E Watmore, et al.
British Journal of Haematology|April 1, 1995
Acute lymphoblastic transformation of essential thrombocythaemiaP T Murphy, M Sivakumaran, F van Rhee, et al.
British Journal of Haematology|May 31, 2001
Fluorescence in situ hybridization analysis of 25 cases of idiopathic myelofibrosis and two cases of secondary myelofibrosis: monoallelic loss of RB1, D13S319 and D13S25 loci associated with cytogenetic deletion and translocation involving 13q14E J Sinclair, E C Forrest, J T Reilly, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Cancer Genetics and Cytogenetics|March 25, 2000
Acute monocytic leukemia with a novel 10;11 rearrangement resolved by fluorescence in situ hybridizationE J Sinclair, S Jalihal, A E Watmore
Cancer Genetics and Cytogenetics|April 15, 1985
Nonendemic Burkitt's lymphoma with complex chromosome abnormalities involving chromosomes 2 and 8A E Watmore, J A Murray, A M Potter
Cancer Genetics and Cytogenetics|January 15, 1985
Value of cytogenetic studies in prediction of acute phase CMLA E Watmore, A M Potter, R J Sokol, et al.
Cancer Genetics and Cytogenetics|July 15, 1988
Methotrexate and bone marrow metaphasesJ J Cunningham, A M Potter, A E Watmore, et al.
Journal of Clinical Pathology|January 1, 1991
Chromosomes in childhood acute lymphoblastic leukaemia: karyotypic patterns in disease subtypesM A Wodzinski, A E Watmore, J S Lilleyman, et al.
Cancer Genetics and Cytogenetics|August 5, 1998
Trisomy 15 associated with loss of the Y chromosome in bone marrow: a possible new aging effectE J Sinclair, A M Potter, A E Watmore, et al.
British Journal of Cancer|July 1, 1981
Significance of non-standard Philadelphia chromosomes in chronic granulocytic leukaemiaA M Potter, A E Watmore, P Cooke, et al.
Cancer Genetics and Cytogenetics|August 25, 1999
Consistent fusion of MOZ and TIF2 in AML with inv(8)(p11q13)M Carapeti, R C Aguiar, A E Watmore, et al.
British Journal of Haematology|April 1, 1995
Acute lymphoblastic transformation of essential thrombocythaemiaP T Murphy, M Sivakumaran, F van Rhee, et al.
British Journal of Haematology|May 31, 2001
Fluorescence in situ hybridization analysis of 25 cases of idiopathic myelofibrosis and two cases of secondary myelofibrosis: monoallelic loss of RB1, D13S319 and D13S25 loci associated with cytogenetic deletion and translocation involving 13q14E J Sinclair, E C Forrest, J T Reilly, et al.
Pageof 2