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Journal Abstract Search

114 related items for PubMed ID: 4064012

  • 1. Chromosome abnormalities in human leukemia as indicators of mutagenic exposure.
    Rowley JD.
    Carcinog Compr Surv; 1985; 10():409-18. PubMed ID: 4064012
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  • 2. Chromosome abnormalities in human acute nonlymphocytic leukemia: relationship to age, sex, and exposure to mutagens.
    Rowley JD.
    Natl Cancer Inst Monogr; 1982; 60():17-23. PubMed ID: 6956808
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  • 3. Clinical implications of cytogenetic abnormalities in acute nonlymphocytic leukemia.
    Trujillo JM, Cork A.
    Am J Pediatr Hematol Oncol; 1981; 3(4):425-31. PubMed ID: 7036783
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  • 4. Cytogenetic and immunologic abnormalities related to leukemia.
    Hirschhorn K.
    Proc Natl Cancer Conf; 1970; 6():107-12. PubMed ID: 5460544
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  • 11. Significance of abnormalities involving chromosomal segment 11q22-25 in acute leukemia.
    Abe R, Sandberg AA.
    Cancer Genet Cytogenet; 1984 Oct; 13(2):121-7. PubMed ID: 6592035
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  • 12. Isochromosome 21 and other chromosomal abnormalities in a patient with erythroleukaemia.
    Werner-Favre C, Cabrol C, Beris P, Engel E.
    Ann Genet; 1983 Oct; 26(4):240-2. PubMed ID: 6607706
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  • 13. Chromosomes and neoplasia.
    Sanger WG.
    Ann Clin Lab Sci; 1983 Oct; 13(5):366-70. PubMed ID: 6227273
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  • 14. Evaluation of chromosome 5 aberrations in complex karyotypes of patients with myeloid disorders reveals their contribution to dicentric and tricentric chromosomes, resulting in the loss of critical 5q regions.
    Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, Morice P, Abgrall JF, Berthou C, De Braekeleer M.
    Cancer Genet Cytogenet; 2007 Jun; 175(2):125-31. PubMed ID: 17556068
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  • 15. [Acute myeloblastic leukemia with involvement of the basophilic cell line and anomalies of the short arm of chromosome 12 (12p)].
    Daniel MT, Bernheim A, Flandrin G, Berger R.
    C R Acad Sci III; 1985 Jun; 301(6):299-301. PubMed ID: 3928106
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  • 16. 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
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