Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder.

J Neurodev Disord · 2011 · PMC3113442 · PMID 21484202

Europe PMC DOI

hedged sentence

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closest p

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boldest claim

The sentences

nominally significantno p-value reported

None of the reported nominally significant associations would survive appropriate correction for multiple comparisons, so these data should be interpreted cautiously.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.