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Common genetic variants, acting additively, are a major source of risk for autism

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The Fragile X Syndrome Protein Represses Activity-Dependent Translation through CYFIP1, a New 4E-BP

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Likelihood-Based Association Analysis for Nuclear Families and Unrelated Subjects with Missing Genotype Data

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Advances in autism genetics: on the threshold of a new neurobiology

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Eukaryotic initiation factor 4E

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