Genome Wide Copy Number Abnormalities in Pediatric Medulloblastomas as Assessed by Array Comparative Genome Hybridization

Array‐based comparative genomic hybridization was used to characterize 22 medulloblastomas in order to precisely define genetic alterations in these malignant childhood brain tumors. The 17p(‐)/17q(+) copy number abnormality (CNA), consistent with the formation of isochromosome 17q, was the most com...

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Detalhes bibliográficos
Publicado no:Brain Pathol
Main Authors: Lo, Ken C., Rossi, Michael R., Eberhart, Charles G., Cowell, John K.
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Publishing Ltd 2007
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8095649/
https://ncbi.nlm.nih.gov/pubmed/17465989
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1750-3639.2007.00072.x
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