Comparative genomic hybridization detects many recurrent imbalances in central nervous system primitive neuroectodermal tumours in children

A series of 23 children with primitive neuroectodermal tumours (PNET) were analysed with comparative genomic hybridization (CGH). Multiple chromosomal imbalances have been detected in 20 patients. The most frequently involved chromosome was chromosome 17, with a gain of 17q (11 cases) and loss of 17...

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Bibliografiske detaljer
Main Authors: Avet-Loiseau, H, Vénuat, A-M, Terrier-Lacombe, M-J, Lellouch-Tubiana, A, Zerah, M, Vassal, G
Format: Artigo
Sprog:Inglês
Udgivet: Nature Publishing Group 1999
Fag:
Regular Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2362778/
https://ncbi.nlm.nih.gov/pubmed/10206302
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.bjc.6690293
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