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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Dettagli Bibliografici
Pubblicato in:Mol Cytogenet
Autori principali: Zagradišnik, Boris, Krgović, Danijela, Herodež, Špela Stangler, Zagorac, Andreja, Ćižmarević, Bogdan, Vokač, Nadja Kokalj
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2018
Soggetti:
Research
Accesso online: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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