Barely Significant
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Rare cases in two Chinese MEN2A families with RET C634Y germline mutation-a homozygous female patient and heterozygous identical twins: a systematic review of literature.

Front Endocrinol (Lausanne) · 2026 · PMC12921576 · PMID 41727686

1
hedged sentence
closest p
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The sentences

a weak trendno p-value reported
Therefore, these data may only suggest a weak trend rather than provide evidence of a true biological effect.

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