- Occurrence of variants of unknown clinical significance in genetic testing for hereditary breast and ovarian cancer syndrome and Lynch syndrome: a literature review and analytical observational retrospective cohort study.
- Adam F, Fluri M, Scherz A, Rabaglio M.
- BMC Med Genomics. 2023 Jan 16;16(1):7. doi: 10.1186/s12920-023-01437-7.
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- Kratz CP, Evans DG.
- Int J Cancer. 2023 Jan 16. doi: 10.1002/ijc.34432. Epub ahead of print.
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The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patients.
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