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Clinical interpretation of CNVs with cross-species phenotype data.
Köhler, Sebastian; Schoeneberg, Uwe; Czeschik, Johanna Christina; Doelken, Sandra C; Hehir-Kwa, Jayne Y; Ibn-Salem, Jonas; Mungall, Christopher J; Smedley, Damian; Haendel, Melissa A; Robinson, Peter N.
Afiliação
  • Köhler S; Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin,Berlin, Germany.
  • Schoeneberg U; Berlin-Brandenburg Center for Regenerative Therapies (BCRT), Berlin, Germany.
  • Czeschik JC; Foundation Institute Molecular Biology and Bioinformatics, Freie Universitaet Berlin, Berlin, Germany.
  • Doelken SC; Institut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, Essen, Germany.
  • Hehir-Kwa JY; Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin,Berlin, Germany.
  • Ibn-Salem J; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Mungall CJ; Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin,Berlin, Germany.
  • Smedley D; Lawrence Berkeley National Laboratory, Berkeley, California, USA.
  • Haendel MA; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, UK.
  • Robinson PN; Department of Medical Informatics and Epidemiology and OHSU Library, Oregon Health & Science University, Portland, USA.
J Med Genet ; 51(11): 766-772, 2014 Nov.
Article em En | MEDLINE | ID: mdl-25280750
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Doença / Variações do Número de Cópias de DNA Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Doença / Variações do Número de Cópias de DNA Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article