Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes.

J Neurodev Disord · 2014 · PMC3995552 · PMID 24628892

Europe PMC DOI

hedged sentence

0.0600

closest p · 1.2× alpha

0.0600

boldest claim

The sentences

marginally significantP =0.06so close (0.05 < p ≤ 0.1)

Linear regression of the executive index did detect a marginally significant group difference ( R 2 =0.10, F (7,120)=1.98, P =0.06).

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