Identification of genomic copy number variations associated with specific clinical features of head and neck cancer

@inproceedings{Zagradinik2018IdentificationOG,
  title={Identification of genomic copy number variations associated with specific clinical features of head and neck cancer},
  author={Boris Zagradi{\vs}nik and Danijela Krgovic and {\vS}pela Stangler Herode{\vz} and Andreja Zagorac and Bogdan {\vC}izmarevi{\vc} and Nadja Kokalj Voka{\vc}},
  booktitle={Molecular Cytogenetics},
  year={2018}
}
BackgroundCopy 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 genomic regions and clinically distinct subgroups of head and neck cancer patients.ResultsArray comparative genomic hybridization (aCGH) analysis was performed on DNA samples in 64 patients with cancer in… CONTINUE READING

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