Frontiers | Minigene Splicing Assays Identify 12 Spliceogenic Variants of BRCA2 Exons 14 and 15 | Genetics
Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes. - Abstract - Europe PMC
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
Germ line BRCA1 pathogenic mutations in breast and ovarian cancer... | Download Table
A computational model for classification of BRCA2 variants using mouse embryonic stem cell-based functional assays | npj Genomic 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
PLOS ONE: Absence of BRCA/FMR1 Correlations in Women with Ovarian Cancers
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
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
Experimentally observed effects on mRNA splicing of group A variants... | Download Table
Novel variants of uncertain clinical significance (VUS) in Greek... | Download Table
Spectrum and frequencies of BRCA1/2 mutations in Bulgarian high risk breast cancer patients – topic of research paper in Biological sciences. Download scholarly article PDF and read for free on CyberLeninka open
Truncating mutations in BRCA1, BRCA2 and PALB2 among 40 TNBC patients. | Download Table
Frontiers | Identification of Eight Spliceogenic Variants in BRCA2 Exon 16 by Minigene Assays | Genetics
Genes | Free Full-Text | Differences in Ovarian and Other Cancers Risks by Population and BRCA Mutation Location | HTML
A Reference System for BRCA Mutation Detection Based on Next-Generation Sequencing in the Chinese Population - The Journal of Molecular Diagnostics
Frameshift mutations detected in BRCA genes | Download Table
PDF] The Clinical Significance of Unknown Sequence Variants in BRCA Genes | Semantic Scholar
PDF) A Python Package for Parsing, Validating, Mapping, and Formatting Sequence Variants Using HGVS Nomenclature
A multi-gene panel study in hereditary breast and ovarian cancer in Colombia | Semantic Scholar
Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project - Genetics in Medicine
Genomic Databases: Emerging Tools for Molecular Diagnostics - ScienceDirect
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] Prevalence and Penetrance of BRCA1 and BRCA2 Germline Mutations in Colombian Breast Cancer Patients | Semantic Scholar