Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker - Wildeman - 2008 - Human Mutation - Wiley Online Library
Figures and data in Functional and mutational landscapes of BRCA1 for homology-directed repair and therapy resistance | eLife
Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis
Genomic Databases: Emerging Tools for Molecular Diagnostics - ScienceDirect
Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project - Genetics in Medicine
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
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
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
![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
Frontiers | Minigene Splicing Assays Identify 12 Spliceogenic Variants of BRCA2 Exons 14 and 15 | Genetics
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PDF] Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas | Semantic Scholar
![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
Experimentally observed effects on mRNA splicing of group A variants... | Download Table
Novel variants of uncertain clinical significance (VUS) in Greek... | Download Table
ENIGMA variant classification process. ENIGMA, Evidence-based Network... | Download Scientific Diagram
A multi-gene panel study in hereditary breast and ovarian cancer in Colombia | Semantic Scholar
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
A computational model for classification of BRCA2 variants using mouse embryonic stem cell-based functional assays | npj Genomic Medicine
Frameshift mutations detected in BRCA genes | 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
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
Online Resource 1A: BRCA1 mutations tested Mutation (BIC
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
PLOS ONE: Absence of BRCA/FMR1 Correlations in Women with Ovarian Cancers
