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Journal Abstract Search

165 related items for PubMed ID: 8194050

  • 21.
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  • 23. Trisomy 4: a specific karyotype anomaly in primary and secondary acute myeloid leukemia.
    Weber E, Nowotny H, Haas OA, Kasparu H, Grois N, Lutz D.
    Leukemia; 1990 Mar; 4(3):219-21. PubMed ID: 2179639
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  • 26. Trisomy 11 acute myeloid leukemia: 5 additional cases from the Japan Adult Leukemia Study Group AML-92 and AML-95 databases.
    Suzuki A, Ohyashiki K, Kimura Y, Yamada H, Sano F, Miyawaki S, Kuriyama K, Ohno R, Japan Adult Leukemia Study Group.
    Int J Hematol; 2000 Dec; 72(4):466-9. PubMed ID: 11197213
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  • 27. MDS and AML with trisomy 8 as the sole chromosome aberration show different sex ratios and prognostic profiles: a study of 115 published cases.
    Pedersen B.
    Am J Hematol; 1997 Dec; 56(4):224-9. PubMed ID: 9395183
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  • 28. Translocations between the long arms of chromosomes 1 and 5 in hematologic malignancies are strongly associated with neoplasms of the myeloid lineages.
    Johansson B, Brøndum-Nielsen K, Billström R, Schiødt I, Mitelman F.
    Cancer Genet Cytogenet; 1997 Dec; 99(2):97-101. PubMed ID: 9398862
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  • 31. Targeted Next-Generation Sequencing in Myelodysplastic Syndrome and Chronic Myelomonocytic Leukemia Aids Diagnosis in Challenging Cases and Identifies Frequent Spliceosome Mutations in Transformed Acute Myeloid Leukemia.
    Reinig E, Yang F, Traer E, Arora R, Brown S, Rattray R, Braziel R, Fan G, Press R, Dunlap J.
    Am J Clin Pathol; 2016 Apr; 145(4):497-506. PubMed ID: 27124934
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  • 32. Clonal cell lineage involvement in myelodysplastic syndromes studied by fluorescence in situ hybridization and morphology.
    Bernell P, Jacobsson B, Nordgren A, Hast R.
    Leukemia; 1996 Apr; 10(4):662-8. PubMed ID: 8618444
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  • 33. Is trisomy 11 another nonrandom chromosomal anomaly in acute nonlymphocytic leukemia and myelodysplastic syndromes?
    Weh HJ, Hoffmann R, Suciu S, Kuse R, Hossfeld DK.
    Cancer Genet Cytogenet; 1988 Oct 15; 35(2):205-11. PubMed ID: 3180022
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  • 35. Transformation of cytogenetically normal chronic myelomonocytic leukaemia to an acute myeloid leukaemia and the emergence of a novel +13, +15 double trisomy resulting in an adverse outcome.
    McGrattan P, Humphreys M, Hull D, McMullin MF.
    Ulster Med J; 2007 Sep 15; 76(3):131-5. PubMed ID: 17853637
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  • 36. Preferential expression of the transcription coactivator HTIF1alpha gene in acute myeloid leukemia and MDS-related AML.
    Gandini D, De Angeli C, Aguiari G, Manzati E, Lanza F, Pandolfi PP, Cuneo A, Castoldi GL, del Senno L.
    Leukemia; 2002 May 15; 16(5):886-93. PubMed ID: 11986951
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  • 37. Systemic mastocytosis with associated clonal hematological non-mast-cell lineage disease: analysis of clinicopathologic features and activating c-kit mutations.
    Pullarkat VA, Bueso-Ramos C, Lai R, Kroft S, Wilson CS, Pullarkat ST, Bu X, Thein M, Lee M, Brynes RK.
    Am J Hematol; 2003 May 15; 73(1):12-7. PubMed ID: 12701114
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  • 39. Clinical significance of isolated del(7p) in myeloid neoplasms.
    Gur HD, Wang SA, Tang Z, Hu S, Li S, Medeiros LJ, Tang G.
    Leuk Res; 2017 Apr 15; 55():18-22. PubMed ID: 28119224
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