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High Resolution X Chromosome Copy Number Variation in Autism
1 de 6
Identification of Aberrantly Expressed Synaptic Proteins in the
Mouse Model of Fragile X Syndrome
2 de 6
Assessment of the clinical impact of sequence variants in the
FMR1 gene
3 de 6
Pathogenesis of novel FMR1 mutations in fragile X syndrome
4 de 6
TET-mediated Hydroxymethylation in Reprogramming to Induced
Pluripotency
5 de 6
An In Vivo Model to Study the Regulation of FMRP
6 de 6