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High frequency of pathogenic germline variants within homologous recombination repair in patients with advanced cancer
Genomic screening of cancer patients for predisposing variants is traditionally based on age at onset, family history and type of cancer. Whereas the clinical guidelines have proven efficient in identifying families exhibiting classical attributes of hereditary cancer, the frequency of patients with...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | NPJ Genom Med |
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| Κύριοι συγγραφείς: | , , , , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Nature Publishing Group UK
2019
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6588611/ https://ncbi.nlm.nih.gov/pubmed/31263571 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41525-019-0087-6 |
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