![PDF] Prevalence and Penetrance of BRCA1 and BRCA2 Germline Mutations in Colombian Breast Cancer Patients | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/3f0ead04db244793e4383a7d82986174e15d367d/5-Table4-1.png "PDF] Prevalence and Penetrance of BRCA1 and BRCA2 Germline Mutations in Colombian Breast Cancer Patients | Semantic Scholar")
PDF] Prevalence and Penetrance of BRCA1 and BRCA2 Germline Mutations in Colombian Breast Cancer Patients | Semantic Scholar
Frontiers | Identification of Eight Spliceogenic Variants in BRCA2 Exon 16 by Minigene Assays | Genetics
Figures and data in Functional and mutational landscapes of BRCA1 for homology-directed repair and therapy resistance | eLife
Experimentally observed effects on mRNA splicing of group A variants... | Download Table
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
dbBRCA - Chinese
Online Resource 1A: BRCA1 mutations tested Mutation (BIC
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
ENIGMA variant classification process. ENIGMA, Evidence-based Network... | Download Scientific Diagram
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
Frontiers | Minigene Splicing Assays Identify 12 Spliceogenic Variants of BRCA2 Exons 14 and 15 | Genetics
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
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
Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project - Genetics in Medicine
Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker - Wildeman - 2008 - Human Mutation - Wiley Online Library
PDF) A Python Package for Parsing, Validating, Mapping, and Formatting Sequence Variants Using HGVS Nomenclature
Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis
Functional Assays for Analysis of Variants of Uncertain Significance in BRCA2 - Guidugli - 2014 - Human Mutation - Wiley Online Library
Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes. - Abstract - Europe PMC
Truncating mutations in BRCA1, BRCA2 and PALB2 among 40 TNBC patients. | Download Table
Genomic Databases: Emerging Tools for Molecular Diagnostics - ScienceDirect
![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")