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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Detalles Bibliográficos
Autores principales: Avet-Loiseau, H, Vénuat, A-M, Terrier-Lacombe, M-J, Lellouch-Tubiana, A, Zerah, M, Vassal, G
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1999
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362778/
https://www.ncbi.nlm.nih.gov/pubmed/10206302
http://dx.doi.org/10.1038/sj.bjc.6690293

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362778/
https://www.ncbi.nlm.nih.gov/pubmed/10206302
http://dx.doi.org/10.1038/sj.bjc.6690293

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