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176 related items for PubMed ID: 12550762

  • 1. Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study.
    Paulsson K, Fioretos T, Strömbeck B, Mauritzson N, Tanke HJ, Johansson B.
    Cancer Genet Cytogenet; 2003 Jan 01; 140(1):66-9. PubMed ID: 12550762
    [Abstract] [Full Text] [Related]

  • 2. High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration.
    Paulsson K, Heidenblad M, Strömbeck B, Staaf J, Jönsson G, Borg A, Fioretos T, Johansson B.
    Leukemia; 2006 May 01; 20(5):840-6. PubMed ID: 16498392
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  • 3. Cytogenetic studies in 112 cases of untreated myelodysplastic syndromes.
    Solé F, Prieto F, Badia L, Woessner S, Florensa L, Caballin MR, Coll MD, Besses C, Sans-Sabrafen J.
    Cancer Genet Cytogenet; 1992 Nov 01; 64(1):12-20. PubMed ID: 1458444
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  • 4. Trisomy 19 as the sole chromosomal anomaly in hematologic neoplasms.
    Johansson B, Billström R, Mauritzson N, Mitelman F.
    Cancer Genet Cytogenet; 1994 May 01; 74(1):62-5. PubMed ID: 8194050
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  • 5. 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 01; 35(1):20-9. PubMed ID: 12203786
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  • 7. 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 01; 10(4):662-8. PubMed ID: 8618444
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  • 8. Partial trisomy 1q. A nonrandom primary chromosomal abnormality in myelodysplastic syndromes?
    Fonatsch C, Haase D, Freund M, Bartels H, Tesch H.
    Cancer Genet Cytogenet; 1991 Oct 15; 56(2):243-53. PubMed ID: 1756470
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  • 9. Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes.
    Paulsson K, Johansson B.
    Pathol Biol (Paris); 2007 Feb 15; 55(1):37-48. PubMed ID: 16697122
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  • 13. A group of previously not recognized cytogenetic abnormalities in myeloid hematological malignancies.
    Chen Z, Richkind K, Roherty S, Velasco J, Lytle C, Brothman AR, Sandberg AA.
    Cancer Genet Cytogenet; 1999 Sep 15; 113(2):162-5. PubMed ID: 10484984
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  • 15. Prognostic significance of del(20q) in patients with hematological malignancies.
    Brezinová J, Zemanová Z, Ransdorfová S, Sindelárová L, Sisková M, Neuwirtová R, Cermák J, Michalová K.
    Cancer Genet Cytogenet; 2005 Jul 15; 160(2):188-92. PubMed ID: 15993278
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  • 16. 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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  • 18. Four additional cases of trisomy 14 as the sole anomaly in various haematological malignancies.
    Brizard A, Guilhot F, Babin P, Burucoa C, Tanzer J, Huret JL.
    Leuk Res; 1992 Jul 15; 16(5):537-40. PubMed ID: 1625480
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  • 19. Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations.
    Heller A, Brecevic L, Glaser M, Loncarevic I, Gebhart E, Claussen U, Liehr T.
    Cancer Genet Cytogenet; 2003 Oct 01; 146(1):81-3. PubMed ID: 14499702
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