Abstract
Since the discovery of the Philadelphia chromosome as a consistent marker for the malignant cells in chronic myelogenous leukemias (1), non random chromosomal changes have been found in several neoplastic diseases of the hematopoietic system (2, 3). Many of these somatic genetic changes involve reciprocal chromosomal traslocations (3), and some have now been shown to occur at or near a proto-oncogene locus. The presence of these chromosomal aberrations have suggested fruitful approaches to the molecular understanding of these tumors. We, therefore, have taken advantage of lymphoid-specific chromosome abnormalities to analyze the mechanisms of oncogenesis in B and T cells on the molecular level.
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Croce, C.M., Gauwerky, C.E. (1991). Molecular Biology of Leukemias and Lymphomas. In: Nicolini, C. (eds) Molecular Basis of Human Cancer. NATO ASI Series, vol 209. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-2563-3_7
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DOI: https://doi.org/10.1007/978-1-4899-2563-3_7
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