Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry

BACKGROUND: Women with breast cancer who have multiple affected relatives are more likely to have inherited genetic risk factors for the disease. All the currently known genetic risk factors for breast cancer account for less than half of the average familial risk. Furthermore, the genetic factor(s)...

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Detalles Bibliográficos
Autores principales: Walker, Logan C., Pearson, John F., Wiggins, George A. R., Giles, Graham G., Hopper, John L., Southey, Melissa C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356248/
https://www.ncbi.nlm.nih.gov/pubmed/28302160
http://dx.doi.org/10.1186/s13058-017-0825-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356248/
https://www.ncbi.nlm.nih.gov/pubmed/28302160
http://dx.doi.org/10.1186/s13058-017-0825-6

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