Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals | Breast Cancer Research | Full Text
Cisplatin with veliparib or placebo in metastatic triple-negative breast cancer and BRCA mutation-associated breast cancer (S1416): a randomised, double-blind, placebo-controlled, phase 2 trial - The Lancet Oncology
The Breast Information Core (BIC) Website Features. Overview and map of... | Download Scientific Diagram
Comparative oncogenomics identifies combinations of driver genes and drug targets in BRCA1-mutated breast cancer | Nature Communications
Identification of the most common BRCA alterations through analysis of germline mutation databases: Is droplet digital PCR an additional strategy for the assessment of such alterations in breast and ovarian cancer families?
Genetics, tumor features and treatment response of breast cancer in Latinas | Breast Cancer Management
Frontiers | Assessing the pathogenicity of BRCA1/2 variants of unknown significance: Relevance and challenges for breast cancer precision medicine
Genes | Free Full-Text | Imprecise Medicine: BRCA2 Variants of Uncertain Significance (VUS), the Challenges and Benefits to Integrate a Functional Assay Workflow with Clinical Decision Rules
The Breast Cancer Information Core: Database design, structure, and scope - Szabo - 2000 - Human Mutation - Wiley Online Library
BRCA1 and BRCA2 genes mutations among high risk breast cancer patients in Jordan | Scientific Reports
![PDF] Genotyping of BRCA 1 , BRCA 2 , p 53 , CDKN 2 A , MLH 1 and MSH 2 genes in a male patient with secondary breast cancer | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c9be17e10dba17347d1fb8b769919e19ce0b43e8/2-Table1-1.png "PDF] Genotyping of BRCA 1 , BRCA 2 , p 53 , CDKN 2 A , MLH 1 and MSH 2 genes in a male patient with secondary breast cancer | Semantic Scholar")
PDF] Genotyping of BRCA 1 , BRCA 2 , p 53 , CDKN 2 A , MLH 1 and MSH 2 genes in a male patient with secondary breast cancer | Semantic Scholar
Spectrum and prevalence of BRCA1/2 germline mutations in Pakistani breast cancer patients: results from a large comprehensive study | Hereditary Cancer in Clinical Practice | Full Text
Addressing health disparities in Hispanic breast cancer: accurate and inexpensive sequencing of BRCA1 and BRCA2 – topic of research paper in Biological sciences. Download scholarly article PDF and read for free on
Diagnostics | Free Full-Text | Male Breast Cancer: Results of the Application of Multigene Panel Testing to an Italian Cohort of Patients
🌸 Join BIC Services in Honouring Breast Cancer Awareness Month! | BIC Services posted on the topic | LinkedIn
BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2 | PLOS Genetics
High prevalence of BRCA1 and BRCA2 mutations in unselected Nigerian breast cancer patients - Fackenthal - 2012 - International Journal of Cancer - Wiley Online Library
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The Breast Information Core (BIC) Website Features. Overview and map of... | Download Scientific Diagram
Genes | Free Full-Text | Prevalence and Spectrum of BRCA Germline Variants in Central Italian High Risk or Familial Breast/Ovarian Cancer Patients: A Monocentric Study
Prevalence of Mutations in the BRCA 1 Gene Among Chinese Patients With Breast Cancer | Semantic Scholar
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Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals | Breast Cancer Research | Full Text
Association between clinical characteristics of breast cancer patients... | Download Table
