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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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| Udgivet i: | Brain Pathol |
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| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Blackwell Publishing Ltd
2007
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| Fag: | |
| Online adgang: | 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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