Abstract
Recent improvements in cytogenetic technology have provided the means to identify chromosomal abnormalities in the majority of children with acute lymphoblastic leukemia (ALL) [4, 18]. In addition to numeric aberrations, specific nonrandom translocations have been described [4, 17]. Cytogenetic studies have also emphasized the clinical significance of chromosomal aberrations in addition to previously identified prognostic factors such as white blood count, sex and age [4, 11, 20]. The applicability of cytogenetic techniques, however, is limited by the laborious and time consuming processing of samples and therefore not suitable for routine clinical evaluations.
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Ritter, J., Hiddemann, W., Wörmann, B., Schellong, G., Büchner, T. (1985). DNA Aneuploidy in Childhood Acute Lymphoblastic Leukemia as Detected by Flow Cytometry: Relation to Phenotype, Presentation Features and Prognosis. In: Büchner, T., Bloomfield, C.D., Hiddemann, W., Hossfeld, D.K., Schumann, J. (eds) Tumor Aneuploidy. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-70458-1_8
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DOI: https://doi.org/10.1007/978-3-642-70458-1_8
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