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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Mol Cytogenet
Päätekijät: Zagradišnik, Boris, Krgović, Danijela, Herodež, Špela Stangler, Zagorac, Andreja, Ćižmarević, Bogdan, Vokač, Nadja Kokalj
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2018
Aiheet:
Research
Linkit: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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