Barely Significant
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Exploratory genetic analysis in children with autism spectrum disorder and other developmental disorders using whole exome sequencing.

Biomol Biomed · 2024 · PMC11293238 · PMID 38421723

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

The sentences

highly significantP < 0.001actually significant
The list of 43 highly significant ( P < 0.001) gene sets was used as input data for GeneNetwork v2.

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