Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach

Cancer, like many common disorders, has a complex etiology, often with a strong genetic component and with multiple environmental factors contributing to susceptibility. A considerable number of genomic variants have been previously reported to be causative of, or associated with, an increased risk...

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Detalles Bibliográficos
Autores principales: Karageorgos, Ioannis, Mizzi, Clint, Giannopoulou, Efstathia, Pavlidis, Cristiana, Peters, Brock A., Zagoriti, Zoi, Stenson, Peter D., Mitropoulos, Konstantinos, Borg, Joseph, Kalofonos, Haralabos P., Drmanac, Radoje, Stubbs, Andrew, van der Spek, Peter, Cooper, David N., Katsila, Theodora, Patrinos, George P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Primary Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499216/
https://www.ncbi.nlm.nih.gov/pubmed/26092435
http://dx.doi.org/10.1186/s40246-015-0034-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499216/
https://www.ncbi.nlm.nih.gov/pubmed/26092435
http://dx.doi.org/10.1186/s40246-015-0034-2

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