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Article

Uptake of predictive testing among relatives of BRCA1 and BRCA2 families: a multicenter study in northeastern Spain.

Familial cancer - 1 Sept 2010

Sanz Judit, Ramón y Cajal Teresa, Torres Asunción, Darder Esther, Gadea Neus, Velasco Angela, Fortuny Daniel, López Consol, Fisas David, Brunet Joan, Alonso M Carmen, Balmaña Judith

Abstract excerpt

Identifying a BRCA mutation among families with hereditary breast and ovarian cancer enables distinguishing those who may benefit from a specific medical management. This study aimed to evaluate the uptake of predictive testing among close relatives of a proband in Spanish families with a BRCA1 or BRCA2 mutation, and to determine the associated demographic and clinical predictors. A retrospective cohort of...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20091130
DOI: 10.1007/s10689-009-9313-1

Genes

BRCA1
BRCA2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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