Barely Significant
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Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder.

Transl Psychiatry · 2013 · PMC3669925 · PMID 23715297

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highly significantno p-value reported
Specific loci on a few chromosomes including three signals on chromosome 3 and one on chromosome 5 yielded the greatest signal, with a sizable percentage of adjacent genes showing highly significant differential expression in blood and brain data from individuals with autism.

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