Classification of missense variants of unknown significance inBRCA1based on clinical and tumor information
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
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1. In Silico and Structure-Based Assessment of Similar Variants Discovered in Tandem Repeats of BRCT Domains of BRCA1 and BARD1 To Characterize the Folding Pattern;ACS Omega;2022-11-28
2. Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883);Journal of Medical Genetics;2020-12-03
3. The BRCA1 c.4096+3A>G Variant Displays Classical Characteristics of Pathogenic BRCA1 Mutations in Hereditary Breast and Ovarian Cancers, But Still Allows Homozygous Viability;Genes;2019-11-01
4. BRCA1/2 germline missense mutations: a systematic review;European Journal of Cancer Prevention;2018-05
5. A Danish national effort of BRCA1/2 variant classification;Acta Oncologica;2017-11-23
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