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Clinical manifestations and spermatogenesis outcomes in Chinese patients with congenital hypogonadotropic hypogonadism caused by inherited or de novo FGFR1 mutations.

Asian J Androl · 2024 · PMC11280213 · PMID 38227553

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a notable trendno p-value reported
Concerning spermatogenesis, the inheritance group displayed a notable trend toward higher success rates and larger testicular volume during follow-up.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.