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- W100488811 abstract "This chapter reviews patterns and clinical and biological significance of genetic changes in neuroblastomas. Patterns based on cytogenetic, molecular, and flow-cytometric analysis that suggest that neuroblastomas can be assigned to three genetically distinct groups. The first comprises those with hyperdiploid or triploid modal karyotypes. The second group consists of tumors that are generally near-diploid or tetraploid modal chromosome number or DNA content. The third group consists of tumors that are also generally near-diploid or tetraploid, with chromosome lp deletion (LOH), with or without double minutes (dmins) or homogenous staining region (HSRs). Studies on the molecular and cytogenetic analysis of human neuroblastomas permit localization of one or more neuroblastoma-predisposition loci. Genetic markers provide a more objective means to classify tumors that may appear similar histologically. In addition, genetic analysis by karyotype, flow cytometry, and the determination of MYCN copy number provides information that has prognostic significance and can direct the most appropriate choice of treatment." @default.
- W100488811 created "2016-06-24" @default.
- W100488811 creator A5004950779 @default.
- W100488811 date "1991-01-01" @default.
- W100488811 modified "2023-09-23" @default.
- W100488811 title "Patterns and Significance of Genetic Changes in Neuroblastomas" @default.
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- W100488811 doi "https://doi.org/10.1016/b978-0-12-564498-3.50011-x" @default.
- W100488811 hasPublicationYear "1991" @default.
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