Access disparities and underutilization of germline genetic testing in Chilean breast cancer patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Oncology
Link
https://link.springer.com/content/pdf/10.1007/s10549-023-06909-z.pdf
Reference31 articles.
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2. Kurian AW, Ward KC, Howlader N, Deapen D, Hamilton AS, Mariotto A et al (2019) Genetic testing and results in a population-based cohort of breast cancer patients and ovarian cancer patients. J Clin Oncol 37:1305–1315. https://doi.org/10.1200/JCO.18.01854
3. Tung N, Battelli C, Allen B, Kaldate R, Bhatnagar S, Bowles K et al (2015) Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel. Cancer 121:25–33. https://doi.org/10.1002/CNCR.29010
4. Makhnoon S, Tran G, Levin B, Mattie KD, Dreyer B, Volk RJ et al (2021) Uptake of cancer risk management strategies among women who undergo cascade genetic testing for breast cancer susceptibility genes. Cancer 127:3605–3613. https://doi.org/10.1002/cncr.33668
5. Beitsch PD, Whitworth PW, Hughes K, Patel R, Rosen B, Compagnoni G et al (2019) Underdiagnosis of hereditary breast cancer: are genetic testing guidelines a tool or an obstacle? J Clin Oncol 37:453–460. https://doi.org/10.1200/JCO.18.01631
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