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1
Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders
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2
Genome-wide screening for DNA variants associated with reading and language traits
Gialluisi, A; Newbury, D F; Wilcutt, E G. - : Blackwell Publishing Ltd, 2014
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3
Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance
In: National Academy of Sciences (U.S.) (2014)
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4
Genome‐wide association analyses of child genotype effects and parent‐of‐origin effects in specific language impairment
Nudel, R.; Simpson, N. H.; Baird, G.. - : Blackwell Publishing Ltd, 2014
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5
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
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6
An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
French, C A; Jin, X; Campbell, T G. - : Nature Publishing Group, 2012
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7
CNTNAP2 variants affect early language development in the general population
Fisher, S E; Whitehouse, A J O; Bishop, D V M. - : Blackwell Publishing Ltd, 2011
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8
CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment
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9
Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment
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10
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia.
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