Barely Significant
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Intra-Familial Phenotypic Heterogeneity and Telomere Abnormality in von Hippel- Lindau Disease: Implications for Personalized Surveillance Plan and Pathogenesis of VHL-Associated Tumors.

Front Genet · 2019 · PMC6491623 · PMID 31068970

Europe PMCDOI
1
hedged sentence
0.0010
closest p · 0.0× alpha
0.0010
boldest claim

The sentences

highly significantp < 0.001actually significant
It turned out that the differences of onset age between different generations and different birth orders were highly significant ( Tables 1 , 3 ) ( p < 0.001).

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