Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders.

Neurol Genet · 2019 · PMC6927359 · PMID 32042908

Europe PMC DOI

hedged sentence

0.0000

closest p · 0.0× alpha

0.0000

boldest claim

The sentences

highly significantp < 0.00001actually significant

These differences are highly significant ( p < 0.00001) whether compared as frequency, average, or normalized by CNV size.

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