Barely Significant
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The frequency of cytomegalovirus non-ELR UL146 genotypes in neonates with congenital CMV disease is comparable to strains in the background population.

BMC Infect Dis · 2021 · PMC8077815 · PMID 33902487

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0.0005
closest p · 0.0× alpha
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highly significantP = 0.0005actually significant
The positive rate was different between the two diagnoses at 34% (55/160) for cCMV and 60% (42/70) for SNHL-CMV, which was a highly significant difference ( P = 0.0005) using Fisher’s exact test.

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