Recurrent gains of 1q, 8 and 12 in the Ewing family of tumours by comparative genomic hybridization.

Comparative genomic hybridization (CGH) was used to detect copy number changes of DNA sequences in the Ewing family of tumours (ET). We analysed 20 samples from 17 patients. Fifteen tumours (75%) showed copy number changes. Gains of DNA sequences were much more frequent than losses, the majority of...

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Bibliographic Details
Main Authors: Armengol, G., Tarkkanen, M., Virolainen, M., Forus, A., Valle, J., Böhling, T., Asko-Seljavaara, S., Blomqvist, C., Elomaa, I., Karaharju, E., Kivioja, A. H., Siimes, M. A., Tukiainen, E., Caballín, M. R., Myklebost, O., Knuutila, S.
Format: Artigo
Language:Inglês
Published: Nature Publishing Group 1997
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC2223493/
https://ncbi.nlm.nih.gov/pubmed/9166930
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