Barely Significant
← all excerpts

Intellectual and Behavioral Phenotypes of Smith-Magenis Syndrome: Comparisons between Individuals with a 17p11.2 Deletion and Pathogenic <i>RAI1</i> Variant.

Genes (Basel) · 2023 · PMC10453904 · PMID 37628566

1
hedged sentence
closest p
boldest claim

The sentences

may be significantno p-value reported
This suggests that variation in FSIQ scores may be significant regardless of genetic subtype.

also in 7,717 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.