Barely Significant
← all excerpts

The Usefulness of a Targeted Next Generation Sequencing Gene Panel in Providing Molecular Diagnosis to Patients With a Broad Spectrum of Neurodevelopmental Disorders.

Front Genet · 2022 · PMC9403311 · PMID 36035117

Europe PMCDOI
1
hedged sentence
0.0370
closest p · 0.7× alpha
0.0370
boldest claim

The sentences

borderline significancep = 0.037actually significant
A higher proportion of females with ID (26.8%) carried causative variants in comparison to males (18.4%) although with a borderline significance ( p = 0.037, Table 2 ).

also in 7,017 other papers

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.