Genotype-phenotype correlations in 9q34.3 microdeletion syndrome: a study of 35 Mainland Chinese patients.

Orphanet J Rare Dis · 2025 · PMC12821790 · PMID 41275302

Europe PMC DOI

hedged sentence

0.1000

closest p · 2.0× alpha

0.1000

boldest claim

The sentences

of borderline significanceP < 0.10so close (0.05 < p ≤ 0.1)

Results were deemed statistically significant at P < 0.05 and of borderline significance at 0.05 < P < 0.10.

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