Barely Significant
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Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study.

Orphanet J Rare Dis · 2016 · PMC4966602 · PMID 27473762

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a strong trendno p-value reported
There was a strong trend to more severe cognitive impairment in patients with Joubert syndrome compared to those with inconclusive MRI, but otherwise no significant difference in clinical phenotypes between these two groups.

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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.