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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Mol Cytogenet
Egile Nagusiak: Zagradišnik, Boris, Krgović, Danijela, Herodež, Špela Stangler, Zagorac, Andreja, Ćižmarević, Bogdan, Vokač, Nadja Kokalj
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2018
Gaiak:
Sarrera elektronikoa: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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