Barely Significant
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The mutational burden and oligogenic inheritance in Klippel-Feil syndrome.

BMC Musculoskelet Disord · 2020 · PMC7149842 · PMID 32278351

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highly significantno p-value reported
These results indicate a highly significant enrichment of predicted damaging genes and the potential oligogenic inheritance of KFS.

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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.