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High Resolution X Chromosome Copy Number Variation in Autism
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Identification of Aberrantly Expressed Synaptic Proteins in the
Mouse Model of Fragile X Syndrome
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Assessment of the clinical impact of sequence variants in the
FMR1 gene
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Pathogenesis of novel FMR1 mutations in fragile X syndrome
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TET-mediated Hydroxymethylation in Reprogramming to Induced
Pluripotency
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An In Vivo Model to Study the Regulation of FMRP
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