Personalised Risk Prediction in Hereditary Breast and Ovarian Cancer: A Protocol for a Multi-Centre Randomised Controlled Trial

SIMPLE SUMMARY: Women with disease-causing gene changes (faults/mutations) in BRCA1, BRCA2, PALB2, CHEK2 and ATM are at an increased risk of developing certain types of cancer—specifically breast (all genes) and epithelial ovarian cancer (only BRCA1, BRCA2, PALB2). At present, the risk estimates giv...

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Detalles Bibliográficos
Autores principales: Archer, Stephanie, Fennell, Nichola, Colvin, Ellen, Laquindanum, Rozelle, Mills, Meredith, Dennis, Romy, Stutzin Donoso, Francisca, Gold, Rochelle, Fan, Alice, Downes, Kate, Ford, James, Antoniou, Antonis C., Kurian, Allison W., Evans, D. Gareth, Tischkowitz, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9179465/
https://www.ncbi.nlm.nih.gov/pubmed/35681696
http://dx.doi.org/10.3390/cancers14112716

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