Barely Significant
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Evaluation of family history in individuals with heterozygous BRCA pathogenic variants diagnosed with breast or ovarian cancer in a single center in Italy.

Mol Genet Genomic Med · 2022 · PMC9747548 · PMID 36307994

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The association between an FH of EOC and a personal history of EOC did not reach statistical significance ( p : .076).

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