Barely Significant
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Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants.

J Am Acad Child Adolesc Psychiatry · 2014 · PMC4074351 · PMID 24954825

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nearly significantno p-value reported
The 3 significant pathways contain different significant genes ( Table 2 and Table S1 ; the latter is available online) despite each pathway containing at least 1 significant gene from the same region on chromosome 16 ( MYH11, NDE1, ABCC1, ABCC6 ), and a significant (or nearly significant) gene from the same region on chromosome 17 ( MYO19, AATF, ACACA ).

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