Common mutation types of BRCA1 or BRCA2 genes in the BIC database. | Download Scientific Diagram
Genes | Free Full-Text | Differences in Ovarian and Other Cancers Risks by Population and BRCA Mutation Location | HTML
Frontiers | Minigene Splicing Assays Identify 12 Spliceogenic Variants of BRCA2 Exons 14 and 15 | Genetics
Recurrent mutation testing of BRCA1 and BRCA2 in asian breast cancer patients identify carriers in those with presumed low risk by family history - Document - Gale OneFile: Health and Medicine
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
Experimentally observed effects on mRNA splicing of group A variants... | Download Table
Novel variants of uncertain clinical significance (VUS) in Greek... | Download Table
Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project - Genetics in Medicine
A computational model for classification of BRCA2 variants using mouse embryonic stem cell-based functional assays | npj Genomic Medicine
ENIGMA variant classification process. ENIGMA, Evidence-based Network... | Download Scientific Diagram
Figures and data in Functional and mutational landscapes of BRCA1 for homology-directed repair and therapy resistance | eLife
PLOS ONE: Absence of BRCA/FMR1 Correlations in Women with Ovarian Cancers
Germline mutational spectrum in Armenian breast cancer patients suspected of hereditary breast and ovarian cancer | Human Genome Variation
Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis
BRCA Exchange
Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes. - Abstract - Europe PMC
Functional Assays for Analysis of Variants of Uncertain Significance in BRCA2 - Guidugli - 2014 - Human Mutation - Wiley Online Library
Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study. - Abstract - Europe PMC
Germ line BRCA1 pathogenic mutations in breast and ovarian cancer... | Download Table
![PDF] Founder BRCA 1 / 2 mutations in the Europe : implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/221cf837a6697343a9d38ca655d37c561e2d8328/11-Table1-1.png "PDF] Founder BRCA 1 / 2 mutations in the Europe : implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar")
PDF] Founder BRCA 1 / 2 mutations in the Europe : implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar
Genomic Databases: Emerging Tools for Molecular Diagnostics - ScienceDirect
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
![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
PDF) A Python Package for Parsing, Validating, Mapping, and Formatting Sequence Variants Using HGVS Nomenclature
