Barely Significant
← all excerpts

Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?

Hum Genomics · 2012 · PMC3528442 · PMID 23244495

1
hedged sentence
0.0000
closest p · 0.0× alpha
0.0000
boldest claim

The sentences

highly significantp = 1.8 × 10 −27actually significant
The results of this analysis, following removal of outliers, revealed a highly significant effect of the mutation type (specifically splice-site mutations) on the number of CALs, both with 1 to 5 CALs ( p = 1.8 × 10 −27 ) and 6 to 99 CALs ( p = 8.5 × 10 −43 ), as well as for skin freckling ( p = 0.028) and neoplasms ( p = 0.006).

also in 82,756 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.