Clinical and genetic features of childhood-onset congenital combined pituitary hormone deficiency: a retrospective, single-center cohort study.

Ann Pediatr Endocrinol Metab · 2024 · PMC11725638 · PMID 39778407

Europe PMC DOI

hedged sentence

0.0590

closest p · 1.2× alpha

0.0590

boldest claim

The sentences

marginal significanceP =0.059so close (0.05 < p ≤ 0.1)

The abnormal MRI group also had lower peak GH levels than the normal MRI group with marginal significance (0.6 ng/mL vs 4.3 ng/mL, P =0.059).

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