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Journal Abstract Search

375 related items for PubMed ID: 12928572

  • 21. Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS/AML.
    Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, De Braekeleer M.
    Eur J Haematol; 2007 Jun; 78(6):457-67. PubMed ID: 17391336
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  • 22. Cytogenetics, in situ hybridization and molecular approaches in the diagnosis of cancer.
    Glassman AB.
    Ann Clin Lab Sci; 1998 Jun; 28(6):324-30. PubMed ID: 9846199
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  • 25. Studies of complex Ph translocations in cases with chronic myelogenous leukemia and one with acute lymphoblastic leukemia.
    Costa D, Carrió A, Madrigal I, Arias A, Valera A, Colomer D, Aguilar JL, Teixido M, Camós M, Cervantes F, Campo E.
    Cancer Genet Cytogenet; 2006 Apr 01; 166(1):89-93. PubMed ID: 16616117
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  • 26. Proposals for standardized protocols for cytogenetic analyses of acute leukemias, chronic lymphocytic leukemia, chronic myeloid leukemia, chronic myeloproliferative disorders, and myelodysplastic syndromes.
    Haferlach C, Rieder H, Lillington DM, Dastugue N, Hagemeijer A, Harbott J, Stilgenbauer S, Knuutila S, Johansson B, Fonatsch C.
    Genes Chromosomes Cancer; 2007 May 01; 46(5):494-9. PubMed ID: 17311250
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  • 27. 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 01; 194(1):30-7. PubMed ID: 19737651
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  • 29. Molecular genetic evidence of Y chromosome loss in male patients with hematological disorders.
    Zhang LJ, Shin ES, Yu ZX, Li SB.
    Chin Med J (Engl); 2007 Nov 20; 120(22):2002-5. PubMed ID: 18067786
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  • 31. 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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  • 32. Do we need to do fluorescence in situ hybridization analysis in myelodysplastic syndromes as often as we do?
    Costa D, Valera S, Carrió A, Arias A, Muñoz C, Rozman M, Belkaid M, Coutinho R, Nomdedeu B, Campo E.
    Leuk Res; 2010 Nov 15; 34(11):1437-41. PubMed ID: 20226525
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  • 34. Chromosomal aberrations in bone marrow mesenchymal stroma cells from patients with myelodysplastic syndrome and acute myeloblastic leukemia.
    Blau O, Hofmann WK, Baldus CD, Thiel G, Serbent V, Schümann E, Thiel E, Blau IW.
    Exp Hematol; 2007 Feb 15; 35(2):221-9. PubMed ID: 17258071
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  • 39. Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases.
    Beyer V, Mühlematter D, Parlier V, Cabrol C, Bougeon-Mamin S, Solenthaler M, Tobler A, Pugin P, Gregor M, Hitz F, Hess U, Chapuis B, Laurencet F, Schanz U, Schmidt PM, van Melle G, Jotterand M.
    Cancer Genet Cytogenet; 2005 Jul 15; 160(2):97-119. PubMed ID: 15993266
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  • 40. [Multiplex fluorescence in situ hybridization in detecting complex chromosomal aberrations in myelodysplastic syndromes].
    Xiao B, Li JY, Pan JL, Ma L, Qiu HR, Wu YF, Xue YQ.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Sep 15; 26(9):513-6. PubMed ID: 16468325
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