Abstract
Cytogenetic analysis of a human embryonal rhabdomyosarcoma revealed a near-diploid karyotype with structural chromosome aberrations not involving the typical rearrangements of rhabdomyosarcomas, plus a large number of double minutes. Comparative genomic hybridization revealed a previously undescribed site of DNA amplification on the short arm of chromosome 1 (band 1p32-33).
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Steilen-Gimbel, H., Remberger, K., Graf, N. et al. A novel site of DNA amplification on chromosome 1p32-33 in a rhabdomyosarcoma revealed by comparative genomic hybridization. Hum Genet 97, 87–90 (1996). https://doi.org/10.1007/BF00218839
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DOI: https://doi.org/10.1007/BF00218839