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Comprehensive prediction of mRNA splicing effects of BRCA1 and BRCA2 variants - Mucaki - 2011 - Human Mutation - Wiley Online Library
Comprehensive prediction of mRNA splicing effects of BRCA1 and BRCA2 variants - Mucaki - 2011 - Human Mutation - Wiley Online Library

ENIGMA variant classification process. ENIGMA, Evidence-based Network... | Download Scientific Diagram
ENIGMA variant classification process. ENIGMA, Evidence-based Network... | Download Scientific Diagram

A computational model for classification of BRCA2 variants using mouse embryonic stem cell-based functional assays | npj Genomic Medicine
A computational model for classification of BRCA2 variants using mouse embryonic stem cell-based functional assays | npj Genomic Medicine

Truncating mutations in BRCA1, BRCA2 and PALB2 among 40 TNBC patients. | Download Table
Truncating mutations in BRCA1, BRCA2 and PALB2 among 40 TNBC patients. | Download Table

Purpose
Purpose

High prevalence of BRCA1 founder mutations in Greek breast/ovarian families
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families

PDF] Novel BRCA1 and BRCA2 genomic rearrangements in Southern Chinese breast/ovarian cancer patients | Semantic Scholar
PDF] Novel BRCA1 and BRCA2 genomic rearrangements in Southern Chinese breast/ovarian cancer patients | Semantic Scholar

A Reference System for BRCA Mutation Detection Based on Next-Generation Sequencing in the Chinese Population - The Journal of Molecular Diagnostics
A Reference System for BRCA Mutation Detection Based on Next-Generation Sequencing in the Chinese Population - The Journal of Molecular Diagnostics

Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes. - Abstract - Europe PMC
Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes. - Abstract - Europe PMC

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
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

Novel variants of uncertain clinical significance (VUS) in Greek... | Download Table
Novel variants of uncertain clinical significance (VUS) in Greek... | Download Table

Absence of BRCA/FMR1 Correlations in Women with Ovarian Cancers
Absence of BRCA/FMR1 Correlations in Women with Ovarian Cancers

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

Functional Assays for Analysis of Variants of Uncertain Significance in BRCA2 - Guidugli - 2014 - Human Mutation - Wiley Online Library
Functional Assays for Analysis of Variants of Uncertain Significance in BRCA2 - Guidugli - 2014 - Human Mutation - Wiley Online Library

BRCA Exchange
BRCA Exchange

Online Resource 1A: BRCA1 mutations tested Mutation (BIC
Online Resource 1A: BRCA1 mutations tested Mutation (BIC

PDF) Novel BRCA1 and BRCA2 pathogenic mutations in Slovene hereditary breast and ovarian cancer families | Petra Cerkovnik - Academia.edu
PDF) Novel BRCA1 and BRCA2 pathogenic mutations in Slovene hereditary breast and ovarian cancer families | Petra Cerkovnik - Academia.edu

Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis – topic of research paper in Biological sciences. Download scholarly article PDF
Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis – topic of research paper in Biological sciences. Download scholarly article PDF

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

Frameshift mutations detected in BRCA genes | Download Table
Frameshift mutations detected in BRCA genes | Download Table

Experimentally observed effects on mRNA splicing of group A variants... | Download Table
Experimentally observed effects on mRNA splicing of group A variants... | Download Table

Genomic Databases: Emerging Tools for Molecular Diagnostics - ScienceDirect
Genomic Databases: Emerging Tools for Molecular Diagnostics - ScienceDirect

Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis
Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis