BRCA1/2 testing: therapeutic implications for breast cancer management | British Journal of Cancer
IJMS | Free Full-Text | Sanger Sequencing for BRCA1 c.68_69del, BRCA1 c.5266dup and BRCA2 c.5946del Mutation Screen on Pap Smear Cytology Samples
A multi-gene panel beyond BRCA1/BRCA2 to identify new breast cancer-predisposing mutations by a picodroplet PCR followed by a next-generation sequencing strategy: a pilot study - ScienceDirect
Cancers | Free Full-Text | Tumor BRCA Testing in High Grade Serous Carcinoma: Mutation Rates and Optimal Tissue Requirements
A Reference System for BRCA Mutation Detection Based on Next-Generation Sequencing in the Chinese Population - The Journal of Molecular Diagnostics
Book an appointment for BRCA Full Gene Sequencing - For Prostate cancer, Breast Cancer & Ovarian Cancer
Frontiers | Management of BRCA Tumour Testing in an Integrated Molecular Tumour Board Multidisciplinary Model
Raed Samara - Next generation sequencing for BRCA1 and BRCA2 mutation testing - YouTube
NEBNext Direct® BRCA1/BRCA2 Panel | NEB
Algorithm of molecular genetic investigation to identify hereditary BRCA -associated breast cancer - Snigireva - Almanac of Clinical Medicine
Pedigree and sequencing results of patient carrying the novel BRCA2... | Download Scientific Diagram
BRCA sequencing of tumors: understanding its implications in the oncology community - Wong - Chinese Clinical Oncology
Promoter methylation and expression changes of BRCA1 in cancerous tissues of patients with sporadic breast cancer
Pathway Genomics bringt BRCA1/2-Gentest mit dem One for One-Programm heraus | Business Wire
Germline BRCA mutation and outcome in young-onset breast cancer (POSH): a prospective cohort study - The Lancet Oncology
Frontiers | Targeting BRCA and DNA Damage Repair Genes in GI Cancers: Pathophysiology and Clinical Perspectives
High-throughput functional evaluation of BRCA2 variants of unknown significance | Nature Communications
Benchmarking of Amplicon-Based Next-Generation Sequencing Panels Combined with Bioinformatics Solutions for Germline BRCA1 and BRCA2 Alteration Detection - ScienceDirect
Frontiers | Prevalence and Spectrum of Germline BRCA1 and BRCA2 Variants of Uncertain Significance in Breast/Ovarian Cancer: Mysterious Signals From the Genome
Identification of the c.829_832delAATA Deletion Variants in the BRCA1 Gene Associated with Hereditary Breast/Ovarian Cancer ˗ Case Report
Investigating the use of Multiple Displacement Amplification (MDA) to amplify nanogram quantities of DNA to use for downstream mutation screening by sequencing. - ppt download
Sanger sequencing of normal homozygous sibling and heterozygous patient... | Download Scientific Diagram
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