Found: 13
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Cancer Spectrum, Family History of Cancer and Overall Survival in Men with Germline BRCA1 or BRCA2 Mutations.
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- Journal of Personalized Medicine, 2021, v. 11, n. 9, p. 917, doi. 10.3390/jpm11090917
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- Article
Knowledge, Attitudes and Referral Patterns of Lynch Syndrome: A Survey of Clinicians in Australia.
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- Journal of Personalized Medicine, 2014, v. 4, n. 2, p. 218, doi. 10.3390/jpm4020218
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- Article
Barriers and Motivators for Referral of Patients with Suspected Lynch Syndrome to Cancer Genetic Services: A Qualitative Study.
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- Journal of Personalized Medicine, 2014, v. 4, n. 1, p. 20, doi. 10.3390/jpm4010020
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- Article
Patient satisfaction after breast cancer surgery: A prospective clinical trial.
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- Wiener Klinische Wochenschrift, 2021, v. 133, n. 1/2, p. 6, doi. 10.1007/s00508-020-01730-w
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- Article
Association between family history, mutation locations, and prevalence of BRCA1 or 2 mutations in ovarian cancer patients.
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- Cancer Medicine, 2019, v. 8, n. 4, p. 1875, doi. 10.1002/cam4.2000
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- Article
Identification and management of familial breast cancer in Austria.
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- Hormone Molecular Biology & Clinical Investigation, 2017, v. 32, n. 2, p. 1, doi. 10.1515/hmbci-2017-0025
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- Article
Improving identification of lynch syndrome patients: A comparison of research data with clinical records.
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- International Journal of Cancer, 2013, v. 132, n. 12, p. 2876, doi. 10.1002/ijc.27978
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- Article
PTEN expression as a predictor for the response to trastuzumab-based therapy in Her-2 overexpressing metastatic breast cancer.
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- PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0172911
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- Article
Performance of clinical risk scores and prediction models to identify pathogenic germline variants in patients with advanced prostate cancer.
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- World Journal of Urology, 2023, v. 41, n. 8, p. 2091, doi. 10.1007/s00345-023-04535-4
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- Article
Cadherin-11 expression is upregulated in invasive human breast cancer.
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- Oncology Letters, 2016, v. 12, n. 6, p. 4393, doi. 10.3892/ol.2016.5236
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- Article
Improving comprehension of genetic counseling for hereditary breast and ovarian cancer clients with a visual tool.
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- PLoS ONE, 2018, v. 13, n. 7, p. 1, doi. 10.1371/journal.pone.0200559
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- Article
Correction: Diagnostic markers for the detection of ovarian cancer in BRCA1 mutation carriers.
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- 2018
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- Correction Notice
Diagnostic markers for the detection of ovarian cancer in BRCA1 mutation carriers.
- Published in:
- PLoS ONE, 2017, v. 12, n. 12, p. 1, doi. 10.1371/journal.pone.0189641
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- Publication type:
- Article