A 29 Mainland Chinese cohort of patients with Phelan-McDermid syndrome: genotype-phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes.

Orphanet J Rare Dis · 2020 · PMC7708101 · PMID 33256793

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 judged to be statistically significant at P < 0.05 and of borderline significance at 0.05 < P < 0.10.

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