Frontiers | Identification of Eight Spliceogenic Variants in BRCA2 Exon 16 by Minigene Assays | Genetics
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
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
PDF] Founder BRCA 1 / 2 mutations in the Europe : implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar
Truncating mutations in BRCA1, BRCA2 and PALB2 among 40 TNBC patients. | Download Table
Functional Assays for Analysis of Variants of Uncertain Significance in BRCA2 - Guidugli - 2014 - Human Mutation - Wiley Online Library
Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker - Wildeman - 2008 - Human Mutation - Wiley Online Library
Novel variants of uncertain clinical significance (VUS) in Greek... | Download Table
Germline mutational spectrum in Armenian breast cancer patients suspected of hereditary breast and ovarian cancer | Human Genome Variation
PDF] Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas | Semantic Scholar
Germ line BRCA1 pathogenic mutations in breast and ovarian cancer... | Download Table
PDF) A Python Package for Parsing, Validating, Mapping, and Formatting Sequence Variants Using HGVS Nomenclature
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis
Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project - Genetics in Medicine
PDF] The Clinical Significance of Unknown Sequence Variants in BRCA Genes | Semantic Scholar
A multi-gene panel study in hereditary breast and ovarian cancer in Colombia | Semantic Scholar
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
A computational model for classification of BRCA2 variants using mouse embryonic stem cell-based functional assays | npj Genomic Medicine
Experimentally observed effects on mRNA splicing of group A variants... | Download Table
dbBRCA - Chinese
Frameshift mutations detected in BRCA genes | Download Table