Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects.

BMC Med Genet · 2014 · PMC3893549 · PMID 24383682

Europe PMC DOI

hedged sentence

0.0600

closest p · 1.2× alpha

0.0600

boldest claim

The sentences

did not reach statistical significanceP = 0.06so close (0.05 < p ≤ 0.1)

Psychiatric disorders were more frequent in the parent group, even though the difference did not reach statistical significance ( P = 0.06).

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