Barely Significant
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Candidate gene linkage approach to identify DNA variants that predispose to preterm birth.

Pediatr Res · 2013 · PMC3740714 · PMID 23168575

Europe PMCDOI
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closest p · 1.0× alpha
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The sentences

nominally significantp =<0.05actually significant
Using TDT, we identified eight nominally significant associated SNPs ( p =<0.05).

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