High prevalence of BRCA1 founder mutations in Greek breast/ovarian families
Prevalence of BRCA1/2 mutations in sporadic breast/ovarian cancer patients and identification of a novel de novo BRCA1 mutation in a patient diagnosed with late onset breast and ovarian cancer: implications for genetic
BRCA genomic rearrangements of the probands | Download Table
BRCA Exchange
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
Germline mutational spectrum in Armenian breast cancer patients suspected of hereditary breast and ovarian cancer | Human Genome Variation
Online Resource 1A: BRCA1 mutations tested Mutation (BIC
![PDF] The Clinical Significance of Unknown Sequence Variants in BRCA Genes | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/bf87f5f3d03688219adbdb700c61ca774b46789f/2-Table1-1.png "PDF] The Clinical Significance of Unknown Sequence Variants in BRCA Genes | Semantic Scholar")
PDF] The Clinical Significance of Unknown Sequence Variants in BRCA Genes | Semantic Scholar
PDF) Novel BRCA1 and BRCA2 pathogenic mutations in Slovene hereditary breast and ovarian cancer families | Petra Cerkovnik - Academia.edu
Comprehensive prediction of mRNA splicing effects of BRCA1 and BRCA2 variants - Mucaki - 2011 - Human Mutation - Wiley Online Library
Purpose
A computational model for classification of BRCA2 variants using mouse embryonic stem cell-based functional assays | npj Genomic Medicine
Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes. - Abstract - Europe PMC
![PDF] Recurrent mutation testing of BRCA1 and BRCA2 in Asian breast cancer patients identify carriers in those with presumed low risk by family history | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/896e5ed721742cc3056bfeeab0ce2d051c8aa65f/8-Table4-1.png "PDF] Recurrent mutation testing of BRCA1 and BRCA2 in Asian breast cancer patients identify carriers in those with presumed low risk by family history | Semantic Scholar")
PDF] Recurrent mutation testing of BRCA1 and BRCA2 in Asian breast cancer patients identify carriers in those with presumed low risk by family history | Semantic Scholar
Truncating mutations in BRCA1, BRCA2 and PALB2 among 40 TNBC patients. | Download Table
Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis – topic of research paper in Biological sciences. Download scholarly article PDF
Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis
The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries - Laitman - 2019 - Human Mutation - Wiley Online Library
Absence of BRCA/FMR1 Correlations in Women with Ovarian Cancers
Frameshift mutations detected in BRCA genes | Download Table
Novel variants of uncertain clinical significance (VUS) in Greek... | Download Table
Spectrum and prevalence of BRCA1/2 germline mutations in Pakistani breast cancer patients: results from a large comprehensive study | SpringerLink
![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
Germ line BRCA1 pathogenic mutations in breast and ovarian cancer... | Download Table
Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women – topic of research paper in Biological sciences. Download scholarly article PDF and read for free
