BIC - Breast Cancer Information Core
Genetic variation and mRNA splicing in familial breast cancer genes | Semantic Scholar
The Breast Information Core (BIC) Website Features. Overview and map of... | Download Scientific Diagram
Mutation and Polymorphism Report
Comparative oncogenomics identifies combinations of driver genes and drug targets in BRCA1-mutated breast cancer | Nature Communications
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
A characterization of genetic haplotypes in BRCA1 identifies linkage disequilibrium with a novel polymorphism in intron 7
BRCA germline mutations in an unselected nationwide cohort of Chinese patients with ovarian cancer and healthy controls - Gynecologic Oncology
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 | HTML
Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast cancer cohort suggests that one-third of mutations are somatic - Annals of Oncology
Abbreviation: BIC, Breast Cancer Information Core database. a GenBank... | Download Scientific Diagram
High prevalence of BRCA1 and BRCA2 mutations in unselected Nigerian breast cancer patients - Fackenthal - 2012 - International Journal of Cancer - Wiley Online Library
BRCA1 mutations occur at the highest rates in the RING domain, exons... | Download Scientific Diagram
BRCA1 and BRCA2 genes mutations among high risk breast cancer patients in Jordan | Scientific Reports
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?
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?
BRCA1/2 testing: therapeutic implications for breast cancer management | British Journal of Cancer
BRCA1/2 variants of unknown significance in hereditary breast and ovarian cancer (HBOC) syndrome: Looking for the hidden meaning - ScienceDirect
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
PDF) Characterization of the c.190T>C missense mutation in BRCA1 codon 64 (Cys64Arg) | Mauro Fasano - Academia.edu
Prevalence and spectrum of BRCA germline variants in mainland Chinese familial breast and ovarian cancer patients | Oncotarget
A novel de novo BRCA1 mutation in a Chinese woman with early onset breast cancer
