Barely Significant
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Enhancing fetal outcomes in GCK-MODY pregnancies: a precision medicine approach via non-invasive prenatal <i>GCK</i> mutation detection.

Front Med (Lausanne) · 2024 · PMC11091329 · PMID 38745742

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failed to reach significanceno p-value reported
Our initial analysis with 259 DNA molecules failed to reach significance, with a likelihood ratio of 605:1, thus inferior to the recommended threshold of 1,200:1 ( 9 ).

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