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5. Molecular rearrangements of the MLL gene are present in most cases of infant acute myeloid leukemia and are strongly correlated with monocytic or myelomonocytic phenotypes. Sorensen PH, Chen CS, Smith FO, Arthur DC, Domer PH, Bernstein ID, Korsmeyer SJ, Hammond GD, Kersey JH. J Clin Invest; 1994 Jan; 93(1):429-37. PubMed ID: 8282816 [Abstract] [Full Text] [Related]
6. Chronic myeloid leukemia with a Philadelphia chromosome involving a t(21;22). Pinkerton PH, London B, Senn JS. Cancer Genet Cytogenet; 1984 Jun; 12(2):175-8. PubMed ID: 6586282 [Abstract] [Full Text] [Related]
13. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH. Schoch C, Haferlach T, Bursch S, Gerstner D, Schnittger S, Dugas M, Kern W, Löffler H, Hiddemann W. Genes Chromosomes Cancer; 2002 Sep; 35(1):20-9. PubMed ID: 12203786 [Abstract] [Full Text] [Related]
14. A myelodysplastic syndrome with marrow eosinophilia terminating in acute nonlymphocytic leukemia, associated with an abnormal chromosome 16. Abbondanzo SL, Gray RG, Whang-Peng J, Jacobson RJ. Arch Pathol Lab Med; 1987 Apr; 111(4):330-2. PubMed ID: 3469939 [Abstract] [Full Text] [Related]
20. 11q- in a case of chronic myelomonocytic leukemia in blastic phase with monoblastic differentiation. Cuneo A, Tomasi P, Balboni M, Castoldi G. Haematologica; 1987 Apr; 72(6):501-4. PubMed ID: 3126105 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]