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Edkins, Sarah

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Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation 179 176 0
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome 216 199 0
Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation 106 102 0
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process 291 265 0
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation 177 132 0
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Edkins, Sarah

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Edkins, Sarah

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