Abstract
Development of immunological methods has made it possible to examine the cellular origin of leukemia cells in relation to their normal counterparts and acute lymphoblastic leukemia (ALL) is generally classified into the following major subgroups: T-ALL, B-ALL and common ALL (cALL) (1). Not infrequently, however, it is impossible to classify acute leukemias as B or T cell or nonlymphoid in origin despite examining lineage associated surface markers, as some malignancies represent stages of differentiation prior to the expression of lineage restricted surface markers. These limitations can now be overcome by utilizing the DNA rearrangement of immunoglobulin (Ig) and T cell receptor genes to reveal the clonality, cellular lineage, and stage of differentiation of such acute undifferentiated leukemias (AUL) (2).
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Raghavachar, A., Bartram, C.R., Kubanek, B. (1986). Immunoglobulin and T-Cell Receptor Gene Rearrangements in Human Acute Leukemias. In: Baum, S.J., Pluznik, D.H., Rozenszajn, L.A. (eds) Experimental Hematology Today—1985. Experimental Hematology Today, vol 1985. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-4920-7_14
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DOI: https://doi.org/10.1007/978-1-4612-4920-7_14
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