Barely Significant
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Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer.

Genet Med · 2015 · PMC4318970 · PMID 25058500

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quite significantno p-value reported
has-supplement yes pmc-prop-pdf-only no pmc-prop-suppress-copyright no pmc-prop-is-real-version no pmc-prop-is-scanned-article no pmc-prop-preprint no pmc-prop-in-epmc yes pmc-license-ref CC BY-NC-ND Introduction Colorectal cancer (CRC) is a very common disease, and its associated mortality rate is quite significant in the developed world.

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