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The RAD51D c.82G>A (p.Val28Met) variant disrupts normal splicing and is associated with hereditary ovarian cancer.
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- Breast Cancer Research & Treatment, 2021, v. 185, n. 3, p. 869, doi. 10.1007/s10549-020-06066-7
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- Article
Counseling About Cancer: Strategies for Genetic Counseling.
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- Psycho-Oncology, 2013, v. 22, n. 11, p. 2636, doi. 10.1002/pon.3431
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- Article
Improved survival for BRCA2-associated serous ovarian cancer compared with both BRCA-negative and BRCA1-associated serous ovarian cancer.
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- Cancer (0008543X), 2012, v. 118, n. 15, p. 3703, doi. 10.1002/cncr.26655
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- Article
Disparities in cancer genetics care by race/ethnicity among pan‐cancer patients with pathogenic germline variants.
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- Cancer (0008543X), 2022, v. 128, n. 21, p. 3870, doi. 10.1002/cncr.34434
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- Article
Comprehensive analysis of germline drivers in endometrial cancer.
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- JNCI: Journal of the National Cancer Institute, 2023, v. 115, n. 5, p. 560, doi. 10.1093/jnci/djad016
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- Article