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
Prevalence and characterization of BRCA1 and BRCA2 germline mutations in Chinese women with familial breast cancer - Document - Gale OneFile: Health and Medicine
Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases | Journal of Translational Medicine | Full Text
Identification of recurrent BRCA1 mutation and its clinical relevance in Chinese Triple-negative breast cancer cohort – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on
Concordance of Genomic Variants in Matched Primary Breast Cancer, Metastatic Tumor, and Circulating Tumor DNA: The MIRROR Study | JCO Precision Oncology
Opportunities and hurdles in the treatment of BRCA1-related breast cancer | Oncogene
Frameshift mutations detected in BRCA genes | Download Table
Research Projects
BRCA1 mutations occur at the highest rates in the RING domain, exons... | Download Scientific Diagram
BIC - Breast Cancer Information Core
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 | HTML
Table 1 from BRCA1 and BRCA2 germline mutations in Korean ovarian cancer patients | Semantic Scholar
BRCA1 And BRCA2 analysis of Argentinean breast/ovarian cancer patients selected for age and family history highlights a role for novel mutations of putative south-American origin – topic of research paper in Biological
![PDF] Identification and evaluation of 55 genetic variations in the BRCA1 and the BRCA2 genes of patients from 50 Japanese breast cancer families | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a8cf6cb2e702aa787d426cca37e549993d924b6d/2-Table1-1.png "PDF] Identification and evaluation of 55 genetic variations in the BRCA1 and the BRCA2 genes of patients from 50 Japanese breast cancer families | Semantic Scholar")
PDF] Identification and evaluation of 55 genetic variations in the BRCA1 and the BRCA2 genes of patients from 50 Japanese breast cancer families | Semantic Scholar
Cancers | Free Full-Text | The Genetic Analyses of French Canadians of Quebec Facilitate the Characterization of New Cancer Predisposing Genes Implicated in Hereditary Breast and/or Ovarian Cancer Syndrome Families | HTML
![PDF] Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/131c15db5c7b7fa8885fd4f7cce9c40d0e09dbb2/11-Table1-1.png "PDF] Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar")
PDF] Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar
PDF) The Breast Cancer Information Core: Database design, structure, and scope
Genes | Free Full-Text | BRCA1/2 Mutations in Vietnamese Patients with Hereditary Breast and Ovarian Cancer Syndrome | HTML
BIC - Breast Cancer Information Core
BRCA2 Deleterious Mutations BIC database, Breast Cancer Information... | Download Table
BRCA1 and BRCA2 mutations in breast cancer patients - SciELO
Mutational analysis of BRCA1 and BRCA2 genes in Peruvian families with hereditary breast and ovarian cancer - Buleje - 2017 - Molecular Genetics & Genomic Medicine - Wiley Online Library
BIC Definition: Breast Cancer Information Core | Abbreviation Finder
