High Resolution X Chromosome Copy Number Variation in Autism
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Associations Between Perinatal Exposures and Neonatal DNA
Methylation
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A Biochemical Model of Hybridization on DNA Microarrays and its Application to Single Nucleotide Polymorphism and Copy Number Variation Genotyping in Trisomy 21 Individuals
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Genetic variation in Down syndrome associated congenital heart
defects
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Stem cell derived monkey neural progenitor cells as a platform for translational research in Huntington's disease
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MeCP2 Mediated Regulation of Small Noncoding RNA
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Genetic variation caused by active retrotransposons in the humangenome
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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