Cancers | Free Full-Text | The Clinical Significance of Unknown Sequence Variants in BRCA Genes | HTML
Investigation of Stereotactic Body Radiation Therapy Delivery Accuracy on an Elekta Linear Accelerator | Semantic Scholar
Integration of functional assay data results provides strong evidence for classification of hundreds of BRCA1 variants of uncertain significance | Genetics in Medicine
Cancers | Free Full-Text | A Functional Analysis of the Unclassified Pro2767Ser BRCA2 Variant Reveals Its Potential Pathogenicity that Acts by Hampering DNA Binding and Homology-Mediated DNA Repair | HTML
A Classification Model Relative to Splicing for Variants of Unknown Clinical Significance: Application to the CFTR Gene - Raynal - 2013 - Human Mutation - Wiley Online Library
IJMS | Free Full-Text | A Case Report of Germline Compound Heterozygous Mutations in the BRCA1 Gene of an Ovarian and Breast Cancer Patient | HTML
IJMS | Free Full-Text | A Case Report of Germline Compound Heterozygous Mutations in the BRCA1 Gene of an Ovarian and Breast Cancer Patient | HTML
Capillary Electrophoresis Analysis of Conventional Splicing Assays: IARC Analytical and Clinical Classification of 31 BRCA2 Genetic Variants - Garibay - 2014 - Human Mutation - Wiley Online Library
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology | Genetics in Medicine
BRCA1 and BRCA2 mutations in a sample of breast and ovarian cancer families from the Colombian pacific
Two Decades After BRCA: Setting Paradigms in Personalized Cancer Care and Prevention | Science
Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk | NEJM
Breast cancer risks associated with missense variants in breast cancer susceptibility genes | medRxiv
Frontiers | MiRNAs: A Powerful Tool in Deciphering Gynecological Malignancies
Visor Redalyc - BRCA1 and BRCA2 mutations in a sample of breast and ovarian cancer families from the Colombian pacific
Genome Annotation by Shotgun Inactivation of a Native Gene in Hemizygous Cells: Application to BRCA2 with Implication of Hypomorphic Variants - Ghosh - 2015 - Human Mutation - Wiley Online Library
Sengvieng Furniture ແສງວຽງເຟີນິເຈີ | Vientiane | Facebook
IJMS | Free Full-Text | Genetic Predisposition to Breast and Ovarian Cancers: How Many and Which Genes to Test? | HTML
Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk | NEJM
Analysis of BRCA1 Variants in Double‐Strand Break Repair by Homologous Recombination and Single‐Strand Annealing - Towler - 2013 - Human Mutation - Wiley Online Library
Growing recognition of the role for rare missense substitutions in breast cancer susceptibility | Biomarkers in Medicine
Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results. - Abstract - Europe PMC
Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approach | European Journal of Human Genetics
Cancers | Free Full-Text | 5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints | HTML
student | Page 136 | Queen's Gazette | Queen's University
