Barely Significant
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Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

Behav Genet · 2011 · PMC3029677 · PMID 21165691

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highly significantno p-value reported
Data cleaning and data handling SNP selection was primarily achieved through a literature review with those highly significant and consistently associated to dyslexia or SLI being prioritised.

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