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Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases

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Juicer Provides a One-Click System for Analyzing Loop-Resolution Hi-C Experiments

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Deletions, Inversions, Duplications: Engineering of Structural Variants using CRISPR/Cas in Mice

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A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping

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Hyperosmia, ectrodactyly, mild intellectual disability, and other defects in a male patient with an X-linked partial microduplication and overexpression of the KAL1 gene

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Refining analyses of copy number variation identifies specific genes associated with developmental delay

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Deletions of exons with regulatory activity at the DYNC1I1 locus are associated with split-hand/split-foot malformation: array CGH screening of 134 unrelated families

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An Integrated Holo-Enhancer Unit Defines Tissue and Gene Specificity of the Fgf8 Regulatory Landscape

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Duplications ofBHLHA9are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion

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Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

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