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Identification of genomic copy number variations associated with specific clinical features of head and neck cancer
BACKGROUND: Copy number variations (CNSs) of large genomic regions are an important mechanism implicated in the development of head and neck cancer, however, for most changes their exact role is not well understood. The aim of this study was to find possible associations between gains/losses of geno...
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| Publicado no: | Mol Cytogenet |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5769503/ https://ncbi.nlm.nih.gov/pubmed/29371888 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-018-0354-8 |
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