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Journal Abstract Search

309 related items for PubMed ID: 10557043

  • 1. Comparison of cytogenetics, Southern blotting, and fluorescence in situ hybridization as methods for detecting MLL gene rearrangements in children with acute leukemia and with 11q23 abnormalities.
    Mathew S, Behm F, Dalton J, Raimondi S.
    Leukemia; 1999 Nov; 13(11):1713-20. PubMed ID: 10557043
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  • 5. Cryptic insertion and translocation or nondividing leukemic cells disclosed by FISH analysis in infant acute leukemia with discrepant molecular and cytogenetic findings.
    Watanabe N, Kobayashi H, Ichiji O, Yoshida MA, Kikuta A, Komada Y, Sekine I, Ishida Y, Horiukoshi Y, Tsunematsu Y, Yano M, Nakadate H, Kaneko Y.
    Leukemia; 2003 May; 17(5):876-82. PubMed ID: 12750700
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  • 7. Detection of MLL gene rearrangements in adult acute lymphoblastic leukemia. A Cancer and Leukemia Group B study.
    Stock W, Thirman MJ, Dodge RK, Rowley JD, Diaz MO, Wurster-Hill D, Sobol RE, Davey FR, Larson RA, Westbrook CA.
    Leukemia; 1994 Nov; 8(11):1918-22. PubMed ID: 7967737
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  • 10. Incidence and characterization of MLL gene (11q23) rearrangements in acute myeloid leukemia M1 and M5.
    Poirel H, Rack K, Delabesse E, Radford-Weiss I, Troussard X, Debert C, Leboeuf D, Bastard C, Picard F, Veil-Buzyn A, Flandrin G, Bernard O, Macintyre E.
    Blood; 1996 Mar 15; 87(6):2496-505. PubMed ID: 8630416
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  • 11. Acute lymphoblastic leukemias with deletion of 11q23 or a novel inversion (11)(p13q23) lack MLL gene rearrangements and have favorable clinical features.
    Raimondi SC, Frestedt JL, Pui CH, Downing JR, Head DR, Kersey JH, Behm FG.
    Blood; 1995 Sep 01; 86(5):1881-6. PubMed ID: 7655016
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  • 13. Frequency and clinical significance of the MLL gene rearrangements in infant acute leukemia.
    Taki T, Ida K, Bessho F, Hanada R, Kikuchi A, Yamamoto K, Sako M, Tsuchida M, Seto M, Ueda R, Hayashi Y.
    Leukemia; 1996 Aug 01; 10(8):1303-7. PubMed ID: 8709635
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  • 14. The t(6;11)(q27;q23) translocation in acute leukemia: a laboratory and clinical study of 30 cases. EU Concerted Action 11q23 Workshop participants.
    Martineau M, Berger R, Lillington DM, Moorman AV, Secker-Walker LM.
    Leukemia; 1998 May 01; 12(5):788-91. PubMed ID: 9593282
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  • 17. MLL translocations with concurrent 3' deletions: interpretation of FISH results.
    Barber KE, Ford AM, Harris RL, Harrison CJ, Moorman AV.
    Genes Chromosomes Cancer; 2004 Nov 01; 41(3):266-71. PubMed ID: 15334550
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  • 18. Granulocytic sarcomas in body cavities in childhood acute myeloid leukemias with 11q23/MLL rearrangements.
    Johansson B, Fioretos T, Kullendorff CM, Wiebe T, Békássy AN, Garwicz S, Forestier E, Roos G, Akerman M, Mitelman F, Billström R.
    Genes Chromosomes Cancer; 2000 Feb 01; 27(2):136-42. PubMed ID: 10612801
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  • 19. Routine fluorescence in situ hybridization with the MLL probe does not reliably detect two separate signals on one chromosome 11 in patients with trisomy 11.
    Smith A, Robson L, Heaps LS, Sharma P, Dunlop L, Bhave A, Bradstock K.
    Cancer Genet Cytogenet; 2001 Sep 01; 129(2):173-6. PubMed ID: 11566351
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  • 20. ALL-1 gene rearrangements in DNA topoisomerase II inhibitor-related leukemia in children.
    Felix CA, Hosler MR, Winick NJ, Masterson M, Wilson AE, Lange BJ.
    Blood; 1995 Jun 01; 85(11):3250-6. PubMed ID: 7756657
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