Found: 10
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Family communication of genetic test results among women with inherited breast cancer genes.
- Published in:
- Journal of Genetic Counseling, 2021, v. 30, n. 3, p. 701, doi. 10.1002/jgc4.1356
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- Publication type:
- Article
An overview of genetic services delivery for hereditary breast cancer.
- Published in:
- Breast Cancer Research & Treatment, 2022, v. 191, n. 3, p. 491, doi. 10.1007/s10549-021-06478-z
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- Publication type:
- Article
Impact of molecular subtype and race on HR+, HER2− breast cancer survival.
- Published in:
- Breast Cancer Research & Treatment, 2021, v. 189, n. 3, p. 845, doi. 10.1007/s10549-021-06342-0
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- Publication type:
- Article
Cancer risk management among female BRCA1/2, PALB2, CHEK2, and ATM carriers.
- Published in:
- Breast Cancer Research & Treatment, 2020, v. 182, n. 2, p. 421, doi. 10.1007/s10549-020-05699-y
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- Publication type:
- Article
Qualitative Methods for Refining a Web-Based Educational Tool for Patients Focused on Inherited Cancer Predisposition.
- Published in:
- Journal of Cancer Education, 2022, v. 37, n. 4, p. 1129, doi. 10.1007/s13187-020-01929-5
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- Publication type:
- Article
IMProving care After inherited Cancer Testing (IMPACT) study: protocol of a randomized trial evaluating the efficacy of two interventions designed to improve cancer risk management and family communication of genetic test results.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Racial disparities in BRCA testing and cancer risk management across a population-based sample of young breast cancer survivors.
- Published in:
- 2017
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- Publication type:
- journal article
Comparing Cancer Risk Management between Females with Truncating CHEK2 1100delC versus Missense CHEK2 I157T Variants.
- Published in:
- Genes, 2024, v. 15, n. 7, p. 881, doi. 10.3390/genes15070881
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- Publication type:
- Article
Breast cancer screening implications of risk modeling among female relatives of ATM and CHEK2 carriers.
- Published in:
- 2020
- By:
- Publication type:
- journal article
The Development and Evaluation of Novel Patient Educational Material for a Variant of Uncertain Significance (VUS) Result in Hereditary Cancer Genes.
- Published in:
- Current Oncology, 2024, v. 31, n. 6, p. 3361, doi. 10.3390/curroncol31060256
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- Publication type:
- Article