Barely Significant
← all excerpts

Genotype-Phenotype Correlations in Children with HHT.

J Clin Med · 2020 · PMC7565052 · PMID 32842615

1
hedged sentence
closest p
boldest claim

The sentences

highly significantno p-value reported
Though our prevalence of the combined phenotype may have been overestimated due to selection bias, the association with an ENG mutation is highly significant and clinically important.

also in 132,142 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.