The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein von Chaganti, Raju S. K, Andresen, J. Michael, Stanton, Vincent P, Behm, Frederick G, Frischauf, Anna Marie, Housman, David E, Watmore, Ann E, Horsman, Doug, Disteche, Christine, Volinia, Stefano, Civin, Curt I, Becher, Reinhard, Mitelman, Felix, Borrow, Julian, Dubé, Ian

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Hematologic malignancies with t(4;11)(q21;q23) : a cytogenetic, morphologic, immunophenotypic and clinical study of 183 cases von JOHANSSON, B, MOORMAN, A. V, HAAS, O. A, WATMORE, A. E, CHEUNG, K. L, SWANTON, S, SECKER-WALKER, L. M

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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 assoc... von Sinclair, E. J., Forrest, E. C., Reilly, J. T., Watmore, A. E., Potter, A. M.

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Cytogenetically cryptic AML1–ETO and CBFβ–MYH11 gene rearrangements: incidence in 412 cases of acute myeloid leukaemia von Rowe, D., Cotterill, S. J., Ross, F. M., Bunyan, D. J., Vickers, S. J., Bryon, J., McMullan, D. J., Griffiths, M. J., Reilly, J. T., Vandenberghe, E. A., Wilson, G., Watmore, A. E., Bown, N. P.

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Chromosomes in childhood acute lymphoblastic leukaemia: karyotypic patterns in disease subtypes von Wodzinski, M A, Watmore, A E, Lilleyman, J S, Potter, A M

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Subpopulations of Colon Cancer Cells Survive Freezing von N. Y. Yaseen, A. E. Watmore, A. M. Potter, Potter, C. W., Jacob, G., Rees, R. C.

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Consistent Fusion of MOZ and TIF2 in AML with inv(8)(p11q13) von Carapeti, Melina, Aguiar, Ricardo C.T, Watmore, Ann E, Goldman, John M, Cross, Nicholas C.P

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Acute Monocytic Leukemia with a Novel 10;11 Rearrangement Resolved by Fluorescence In Situ Hybridization von Sinclair, Elizabeth J, Jalihal, Sanjeev, Watmore, Ann E

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Trisomy 15 Associated with Loss of the Y Chromosome in Bone Marrow: A Possible New Aging Effect von Sinclair, Elizabeth J., Potter, Anthony M., Watmore, Ann E., Fitchett, Margaret, Ross, Fiona

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Der(6)t(1;6)(q21–23;p21.3): a specific cytogenetic abnormality in myelofibrosis with myeloid metaplasia von Dingli, David, Grand, Francis H., Mahaffey, Victor, Spurbeck, Jack, Ross, Fiona M., Watmore, Ann E., Reilly, John T., Cross, Nicholas C. P., Dewald, Gordon W., Tefferi, Ayalew

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Methotrexate and bone marrow metaphases von Cunningham, J.J.P., Potter, A.M., Watmore, A.E., Winfield, D.A.

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Value of cytogenetic studies in prediction of acute phase CML von Watmore, A.E., Potter, A.M., Sokol, R.J., Wood, J.K.

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Chromosome studies in eleven colorectal tumors von Yaseen, N.Y., Watmore, A.E., Potter, A.M., Potter, C.W., Jacob, G., Rees, R.C.

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Significance of non-standard Philadelphia chromosomes in chronic granulocytic leukaemia von Potter, A M, Watmore, A E, Cooke, P, Lilleyman, J S, Sokol, R J

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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 von Sinclair, E J, rest, E C, Reilly, J T, Watmore, A E, Potter, A M

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Cytogenetically cryptic AML1-ETO and CBFbeta-MYH11 gene rearrangements: incidence in 412 cases of acute myeloid leukaemia von Rowe, D., Cotterill, S. J., Ross, F. M., Bunyan, D. J., Vickers, S. J., Bryon, J., McMullan, D. J., Griffiths, M. J., Reilly, J. T., Vandenberghe, E. A., Wilson, G., Watmore, A. E., Bown, N. P.

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Hematologic malignancies with t(4;11)(q21;q23)--a cytogenetic, morphologic, immunophenotypic and clinical study of 183 cases. European 11q23 Workshop participants von Johansson, B, Moorman, A V, Haas, O A, Watmore, A E, Cheung, K L, Swanton, S, Secker-Walker, L M

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Cytogenetically crytic AML1-ETO and CBFβ-MYH11 gene rearrangements: incidence in 412 cases of acute myeloid leukaemia von ROWE, D, COTTERILL, S. J, WILSON, G, WATMORE, A. E, BOWN, N. P, ROSS, F. M, BUNYAN, D. J, VICKERS, S. J, BRYON, J, MCMULLAN, D. J, GRIFFITHS, M. J, REILLY, J. T, VANDENBERGHE, E. A

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Loss of the Y chromosome from normal and neoplastic bone marrows

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Nonendemic Burkitt's lymphoma with complex chromosome abnormalities involving chromosomes 2 and 8 von Watmore, Ann E., Murray, J.A., Potter, A.M.

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