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Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders
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Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment
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In: Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment (2017)
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Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
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In: Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes (2016)
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Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
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In: Symplectic Elements at Oxford ; Added by author ; ORA review team (2016)
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Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.
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Genome-wide screening for DNA variants associated with reading and language traits
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Genome‐wide association analyses of child genotype effects and parent‐of‐origin effects in specific language impairment
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Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
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A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3
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CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment
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Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment
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