Φορτώνει......
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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Mol Cytogenet |
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| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2018
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| Θέματα: | |
| Διαθέσιμο 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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