Barely Significant
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Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism.

Genome Med · 2024 · PMC11429951 · PMID 39334436

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a decreasing trendno p-value reported
Although we were not able to identify a decrease in the sex ratio depending on increasing total symptom severity in a consistent manner in the Korean cohort, we observed a decreasing trend in that ratio for individuals with autism and ID (6.2 for normative cases; 3.3 for severe cases; OR = 1.91; 95% CI = 0.88–4.63) (Fig. 4 B).

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