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Copy number variation screen identifies a rare de novo deletion at chromosome 15q13.1-13.3 in a child with language impairment
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2 |
Genome-wide screening for DNA variants associated with reading and language traits
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3 |
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
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4 |
Reading and language disorders : the importance of both quantity and quality
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