Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help?

Background: Detection of variants of uncertain significance (VUSs) in BRCA1 and BRCA2 genes poses relevant challenges for counseling and managing patients. VUS carriers should be managed similarly to probands with no BRCA1/2 variants detected, and predictive genetic testing in relatives is discourag...

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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Zuntini, Roberta, Ferrari, Simona, Bonora, Elena, Buscherini, Francesco, Bertonazzi, Benedetta, Grippa, Mina, Godino, Lea, Miccoli, Sara, Turchetti, Daniela
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2018
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6141711/
https://ncbi.nlm.nih.gov/pubmed/30254663
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2018.00378
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