- [Line 17535]Rowley, J.D. (1993) "Rearrangements involving chromosome band 11q23 in acute leukemia". Seminars in Cancer Biology 4, 377-385.
- [Line 17563]Cimino, G., Rapanoli, M.C., Rivolta, A., LoCoco, F., D'Arcangelo, E., Rondelli, R., Basso, G., Barisone, E., Rosaada, C., Scinlostasi, T., Canaani, F., Masera, G., Mandelli, F. and Biondi, A. (1995) "Prognostic relevance of ALL-1 gene rearrangement in infant acute leukemias". Leukemia 9, 3391-3395
- [Line 17604]Heim, S. and Mitelman, F. (1992) "Cytogenelic analysis in the diagnosis of acute leukemia", Cancer 70, 1701-1709.
- [Line 17633]Bredeson, C.N., Barnett, M.J., Horsman, U.K., Dalal, B.I., Ragaz., J. and Philips, G.L. (1993) "Therapy related acute myelogenous leukemia associated with 11q23 chromosomal abnormalities and topoisomerasc Il inhibitors: report of four additional cases and brief commentary". Leukemia and Lymphoma 11, 141-145.
- [Line 17666]Harrison, C.J., Cuneo. A., Clark, R., Johansson, B., LafagePochitaloff, M., Mugneret, F., Moorman, A.V. and Seeker-Walker, L.M. (1998) "Ten novel 11q23 chromosomal partner sites". Leukemia 12, 811-822.
- [Line 17701]Seeker-Walker, L.M., Moorman, A.V., Rain, B.J. and Mehta, A.B. (1998) "Secondary acute leukemia and myelodysplastic syndrome with 11q23 abnormalities. EU concerted Action 11q23 Workshop". Leukemia 12, 840-844.
- [Line 17732]Kwong, Y.L. (1997) "Partial duplication of the MLL gene in acute myelogenous leukemia without karyotypic aberration". Cancer Genetics and Cytogenetics 97, 20-24
- [Line 17760]Streubel, B., Valent, P., Jäger, U., Edelhäuser, M., Wandt, H., Wagner, T., Büchner. T., Lechner, K. and Fonatsch, Ch. (2000) "Amplification of the MLL gene on double minutes, a homogeneously staining region, and ring chromosomes in five patients with acute myeloid leukemia or myelodysnlastic syndrome", Genes Chromaxomes and Cancer 27, 380-386.
- [Line 17796]Rowley, J.D. (1993) "Rearrangements involving chromosome band 11q23 in acute leukemia". Seminars in Cancer Biology 4, 377-385.
- [Line 17824]Cimino, G., Rapanoli, M.C., Rivolta, A., LoCoco, F., D'Arcangelo, E., Rondelli, R., Basso, G., Barisone, E., Rosaada, C., Scinlostasi, T., Canaani, F., Masera, G., Mandelli, F. and Biondi, A. (1995) "Prognostic relevance of ALL-1 gene rearrangement in infant acute leukemias". Leukemia 9, 3391-3395
- [Line 17865]Heim, S. and Mitelman, F. (1992) "Cytogenelic analysis in the diagnosis of acute leukemia", Cancer 70, 1701-1709.
- [Line 17894]Bredeson, C.N., Barnett, M.J., Horsman, U.K., Dalal, B.I., Ragaz., J. and Philips, G.L. (1993) "Therapy related acute myelogenous leukemia associated with 11q23 chromosomal abnormalities and topoisomerasc Il inhibitors: report of four additional cases and brief commentary". Leukemia and Lymphoma 11, 141-145.
- [Line 17927]Harrison, C.J., Cuneo. A., Clark, R., Johansson, B., LafagePochitaloff, M., Mugneret, F., Moorman, A.V. and Seeker-Walker, L.M. (1998) "Ten novel 11q23 chromosomal partner sites". Leukemia 12, 811-822.
- [Line 17962]Seeker-Walker, L.M., Moorman, A.V., Rain, B.J. and Mehta, A.B. (1998) "Secondary acute leukemia and myelodysplastic syndrome with 11q23 abnormalities. EU concerted Action 11q23 Workshop". Leukemia 12, 840-844.
- [Line 17993]Kwong, Y.L. (1997) "Partial duplication of the MLL gene in acute myelogenous leukemia without karyotypic aberration". Cancer Genetics and Cytogenetics 97, 20-24
- [Line 18021]Streubel, B., Valent, P., Jäger, U., Edelhäuser, M., Wandt, H., Wagner, T., Büchner. T., Lechner, K. and Fonatsch, Ch. (2000) "Amplification of the MLL gene on double minutes, a homogeneously staining region, and ring chromosomes in five patients with acute myeloid leukemia or myelodysnlastic syndrome", Genes Chromaxomes and Cancer 27, 380-386.
- [Line 18057]Park, J.P., Ladd, S.L., Ely, P., Weiner, A.J., Wojiski, S. A., Hawk. A.B., Noll, W.W. and Mohandas, T.K. (2000) "Amplification of the MLL region in acute myeloid leukemia". Cancer Genetics and Cytogenetics 121, 198-205.
- [Line 18092]Michalová K., Ccrmák, J., Bewnová, J. and Zemanová, Z. (1999) "Double minute chromosomes in a patient with myelodysplastic syndrome transforming into acute myeloid leukemia". Cancer Genetics and Cytogenetics 109, 76-78.
- [Line 18123]Yunis, J.J. (1981) "New chromosome techniques in the study of human neoplasia". Human Pathology 12, 540-549.
- ISCN (1995) In: Mitelman, F., eds. An International System for Human Cytogenetic Nomenclature (Karger. Basel).
- Hesketh, R. (1997) The Oncogene and Tumour Suppressor Gene, 2nd Ed. (Academic Press, London. UK).
- [Line 18197]Tanaka, K., Takechi, M., Nishimura, S., Oguma, A. and Kamada, A. (1993) "Amplification of c-mye oncogene in acute myelocytic leukemia with double minute chromosomes". Leukemia 7, 469-473.
- [Line 18229]Schichman, S.A., Caligiuri, M.A., Strout, M.P., Carter, S.L., Gu, Y. Canaani, K., Bloomfield, C.D. and Croce, C.M. (1994) "ALL-1 tandem duplication in acute myeloid leukemia with a normal karyotype involves homologous recombination between alu elements". Cancer Research 54, 4277-4280.
- [Line 18264]Bernard, O.A., Romana, S.P., Schichman, S.A., Mauchauffe, M., Jonveaux, P. and Berger, R. (1995) "Partial duplication of HRX in acute leukemia with trisomy 11", Leukemia 9, 1487-1490.
- [Line 18297]Andersen, M.K. Christiansen, D.H., Kirchhoff, M. and PedersenBjergaard, J. (2001) "Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML. and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents". Genes, Chromosomes and Cancer 31, 33-41.
- [Line 18328]Cuthbert,. G., Thompson, K., McCullough, S., Watmore, A., Dickinson, H., Telford, N., Mugneret, F., Harrison, C., Griffiths, M. and Bown, N. (2000) "MLL amplification in acute leukemia: a United Kingdom Cancer Cytogeneties Group (UKCCG) study". Leukemia 14, 1885-1891.
Variations in MLL Amplification in a Patient with Acute Myeloid Leukemia
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