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Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders
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Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders
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In: Biochemistry and Microbiology (2016)
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The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains
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Genome-wide screening for DNA variants associated with reading and language traits
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Quantitative-trait locus for specific language and reading deficits on chromosome 6p.
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