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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

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
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

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
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

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

Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project - Genetics in Medicine
Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project - Genetics in Medicine

dbBRCA - Chinese
dbBRCA - Chinese

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

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

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

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

GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS

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
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

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

Germline mutational spectrum in Armenian breast cancer patients suspected of hereditary breast and ovarian cancer | Human Genome Variation
Germline mutational spectrum in Armenian breast cancer patients suspected of hereditary breast and ovarian cancer | Human Genome Variation

Common mutation types of BRCA1 or BRCA2 genes in the BIC database. | Download Scientific Diagram
Common mutation types of BRCA1 or BRCA2 genes in the BIC database. | Download Scientific Diagram

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

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
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

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

GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS

BRCA Exchange
BRCA Exchange

A multi-gene panel study in hereditary breast and ovarian cancer in Colombia | Semantic Scholar
A multi-gene panel study in hereditary breast and ovarian cancer in Colombia | Semantic Scholar

PDF] Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas | Semantic Scholar
PDF] Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas | Semantic Scholar

Figures and data in Functional and mutational landscapes of BRCA1 for homology-directed repair and therapy resistance | eLife
Figures and data in Functional and mutational landscapes of BRCA1 for homology-directed repair and therapy resistance | eLife