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Human genome / Copy-number variation / Gene / Ridge / Lac operon / House mouse / Biology / Genetics / Potocki-Lupski syndrome


Phenotypic Consequences of Copy Number Variation: Insights from Smith-Magenis and Potocki-Lupski Syndrome Mouse Models
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Document Date: 2011-03-17 21:28:57

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Houston / Valdivia / Lausanne / /

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Rai / Empresas CMPC / Antofagasta / Creative Commons / /

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Switzerland / Chile / United States / /

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University of Miami Miller School / Swiss Institute of Bioinformatics / Baylor College of Medicine / Texas Children’s Hospital / University of Lausanne / John P. Hussman Institute / /

MedicalCondition

Potocki-Lupski syndrome / overt seizures / Smith-Magenis Syndrome / hypertelorism / craniofacial abnormalities / Information Figure S1 Neuromotor dysfunction / autism spectrum disorder / obesity / CIN / Figure S2 Craniofacial abnormalities / hearing loss / dissociation / schizophrenia / disease / genomic disorders / diseases / normal normal Craniofacial abnormalities / /

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B2 / MMU11B2 / /

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eQTL association / Chilean Government / University of Miami Miller School of Medicine / Miami / John P. Hussman Institute for Human Genomics / Medical Research Council Human Genetics Unit / Center for Integrative Genomics / Baylor College of Medicine / Houston / Telethon Action Suisse Foundation / Swiss Institute of Bioinformatics / Je´roˆme Lejeune Foundation / European Commission / Texas Children’s Hospital / Swiss National Science Foundation / University of Lausanne / Lausanne / /

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original author / Author / Academic Editor / /

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Texas / Florida / Arkansas / /

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PLoS Biology / /

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Genomics / Bioinformatics / SMS / Genotyping / human genome / PDF / DNA Chip / gene expression / genotype / recombination / /

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