Copy Number Variants in Candidate Genes Are Genetic Modifiers of Hirschsprung Disease

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Differential Contributions of Rare and Common, Coding and Noncoding Ret Mutations to Multifactorial Hirschsprung Disease Liability

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Copy number variation modifies expression time courses

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Diversity of Human Copy Number Variation and Multicopy Genes

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Duplications Involving a Conserved Regulatory Element Downstream of BMP2 Are Associated with Brachydactyly Type A2

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Analysis ofRET,ZEB2,EDN3andGDNFGenomic Rearrangements in 80 Patients with Hirschsprung Disease (Using multiplex ligation-dependent probe amplification)

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A novel study of Copy Number Variations in Hirschsprung disease using the Multiple Ligation-dependent Probe Amplification (MLPA) technique

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Interaction between a chromosome 10RETenhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association

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Duplications of noncoding elements 5′ of SOX9 are associated with brachydactyly-anonychia

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Genome-wide association study identifiesNRG1as a susceptibility locus for Hirschsprung's disease

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High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians

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The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1

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