Barely Significant
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Exome first approach to reduce diagnostic costs and time - retrospective analysis of 111 individuals with rare neurodevelopmental disorders.

Eur J Hum Genet · 2022 · PMC8738730 · PMID 34690354

Europe PMCDOI
1
hedged sentence
0.0010
closest p · 0.0× alpha
0.0010
boldest claim

The sentences

highly significantp < 0.001actually significant
While only a relatively weak significant difference ( p ~ 0.03, Wilcox-Test) was found for individuals with first symptoms before April 2016, a highly significant difference ( p < 0.001, Wilcox-Test) was found for individuals with first symptoms after 2016.

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