BRIP1, RAD51C, and RAD51D mutations are associated with high susceptibility to ovarian cancer: mutation prevalence and precise risk estimates based on a pooled analysis of ~30,000 cases | Journal of Ovarian Research
Domain structure of PALB2 and RAD51C. The amino acid numbers are listed... | Download Scientific Diagram
RAD51C – Inherited Cancer Registry (ICARE)
A dominant RAD51C pathogenic splicing variant predisposes to breast and ovarian cancer in the Newfoundland population due to founder effect - Dawson - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library
RAD51C Gene - GeneCards | RA51C Protein | RA51C Antibody
Figure 5 from The Role of rad51c on the Fanconi Anemia Pathway in Zebrafish | Semantic Scholar
Genes | Free Full-Text | RAD-ical New Insights into RAD51 Regulation
What is RAD51C Gene Breast-ovarian cancer NGS Genetic DNA Test ?
Homologous recombination–deficient mutation cluster in tumor suppressor RAD51C identified by comprehensive analysis of cancer variants | PNAS
Cancer risk and RAD51C gene mutations
Cancers | Free Full-Text | Analysis of BRCA1 and RAD51C Promoter Methylation in Italian Families at High-Risk of Breast and Ovarian Cancer
BR_RAD51C - AMIOMICS
RAD51C Gene - GeneCards | RA51C Protein | RA51C Antibody
A decade of RAD51C and RAD51D germline variants in cancer - Boni - 2022 - Human Mutation - Wiley Online Library
RAD51C (RAD51 paralog C) | Gene Report | BioGPS
Gene‐panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication - Pelttari - 2018 - Clinical Genetics - Wiley Online Library
RAD51C – Inherited Cancer Registry (ICARE)
US firm corners exclusive license for RAD51C cancer gene - The Lancet Oncology
spn-D encodes a Rad51C-like protein . (A) spn-D gene structure .... | Download Scientific Diagram
Generation of Rad51C mutant cells by gene targeting. (A) Strategy for... | Download Scientific Diagram
RAD51C Gene - GeneCards | RA51C Protein | RA51C Antibody
Homologous recombination–deficient mutation cluster in tumor suppressor RAD51C identified by comprehensive analysis of cancer variants | PNAS
