Barely Significant
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Functional annotation of genes overlapping copy number variants in autistic patients: focus on axon pathfinding.

Curr Genomics · 2010 · PMC2874223 · PMID 20885821

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highly significantno p-value reported
Several networks with highly significant scores were obtained for each of the three CS2 gene lists (“all”, “gain”, “loss”) (not shown).

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