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416 related items for PubMed ID: 15474149

  • 1. Interphase fluorescence in situ hybridization studies for the detection of 9q34 deletions in chronic myelogenous leukemia: a practical approach to clinical diagnosis.
    Aoun P, Wiggins M, Pickering D, Foran J, Rasheed H, Pavletic SZ, Sanger W.
    Cancer Genet Cytogenet; 2004 Oct 15; 154(2):138-43. PubMed ID: 15474149
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  • 9. Molecular cytogenetic characterization of variant Philadelphia translocations in chronic myeloid leukemia: genesis and deletion of derivative chromosome 9.
    Bennour A, Sennana H, Laatiri MA, Elloumi M, Khelif A, Saad A.
    Cancer Genet Cytogenet; 2009 Oct 15; 194(1):30-7. PubMed ID: 19737651
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  • 11. [Study of deletion of derivative chromosome 9 in patients with Ph+ chronic myeloid leukemia].
    Wu W, Xue YQ, Wu YF, Pan JL, Shen J.
    Zhonghua Xue Ye Xue Za Zhi; 2006 Mar 15; 27(3):183-6. PubMed ID: 16792921
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  • 12. Application of fluorescence in situ hybridization in defining a complex t(9;21;22) Ph formation.
    Mancini M, Nanni M, Cedrone M, De Cuia MR, Rondinelli MB, Malagnino F, Alimena G.
    Haematologica; 1994 Mar 15; 79(6):536-9. PubMed ID: 7896212
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  • 13. Molecular cytogenetic characterization of deletions on der(9) in chronic myelocytic leukemia.
    Zagaria A, Anelli L, Albano F, Vicari L, Schiavone EM, Annunziata M, Pane F, Liso V, Rocchi M, Specchia G.
    Cancer Genet Cytogenet; 2006 Jun 15; 167(2):97-102. PubMed ID: 16737907
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  • 14. A complex translocation t(5;9;22) in Philadelphia cells involving the short arm of chromosome 5 in a case of chronic myelogenous leukemia.
    Al-Achkar W, Wafa A, Nweder MS.
    J Exp Clin Cancer Res; 2007 Sep 15; 26(3):411-5. PubMed ID: 17987804
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  • 15. A dual colour dual fusion fluorescence in situ hybridisation study on the genesis of complex variant translocations in chronic myelogenous leukaemia.
    So CC, Wan TS, Yip SF, Chan LC.
    Oncol Rep; 2008 May 15; 19(5):1181-4. PubMed ID: 18425374
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  • 17. Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases.
    Albano F, Specchia G, Anelli L, Zagaria A, Storlazzi CT, Buquicchio C, Roberti MG, Liso V, Rocchi M.
    Genes Chromosomes Cancer; 2003 Apr 15; 36(4):353-60. PubMed ID: 12619159
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  • 18. [Molecular genetics in chronic myeloid leukemia with variant Ph translocation].
    Wu W, Li JY, Zhu Y, Qiu HR, Pan JL, Xu W, Chen LJ, Shen YF, Xue YQ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug 15; 24(4):470-3. PubMed ID: 17680547
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  • 20. A two-color BCR-ABL probe that greatly reduces the false positive and false negative rates for fluorescence in situ hybridization in chronic myeloid leukemia.
    Grand FH, Chase A, Iqbal S, Nguyen DX, Lewis JL, Marley SB, Davidson RJ, Goldman JM, Gordon MY.
    Genes Chromosomes Cancer; 1998 Oct 15; 23(2):109-15. PubMed ID: 9739013
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