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Association between family history, mutation locations, and prevalence of BRCA1 or 2 mutations in ovarian cancer patients

We investigated the prevalence of germline BRCA mutations in a population‐based cohort of Austrian women diagnosed with ovarian cancer and its association with family history of cancer. We prospectively collected family pedigrees of 443 Austrian ovarian cancer patients who had been tested for the pr...

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Podrobná bibliografie
Vydáno v:Cancer Med
Hlavní autoři: Singer, Christian F., Tan, Yen Y., Muhr, Daniela, Rappaport, Christine, Gschwantler‐Kaulich, Daphne, Grimm, Christoph, Polterauer, Stephan, Pfeiler, Georg, Berger, Andreas, Tea, Muy‐Kheng M.
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2019
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6488144/
https://ncbi.nlm.nih.gov/pubmed/30821131
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cam4.2000
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