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Disease insights through cross-species phenotype comparisons.
Haendel, Melissa A; Vasilevsky, Nicole; Brush, Matthew; Hochheiser, Harry S; Jacobsen, Julius; Oellrich, Anika; Mungall, Christopher J; Washington, Nicole; Köhler, Sebastian; Lewis, Suzanna E; Robinson, Peter N; Smedley, Damian.
Afiliação
  • Haendel MA; University Library and Department of Medical Informatics and Epidemiology, Oregon Health & Science University, Portland, OR, USA.
  • Vasilevsky N; University Library and Department of Medical Informatics and Epidemiology, Oregon Health & Science University, Portland, OR, USA.
  • Brush M; University Library and Department of Medical Informatics and Epidemiology, Oregon Health & Science University, Portland, OR, USA.
  • Hochheiser HS; Department of Biomedical Informatics and Intelligent Systems Program, University of Pittsburgh, Pittsburgh, PA, 15206, USA.
  • Jacobsen J; Skarnes Faculty Group, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.
  • Oellrich A; Skarnes Faculty Group, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.
  • Mungall CJ; Genomics Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA, 94720, USA.
  • Washington N; Genomics Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA, 94720, USA.
  • Köhler S; Computational Biology Group, Institute for Medical Genetics and Human Genetics, Universitatsklinikum Charité, Augustenburger Platz 1, 13353, Berlin, Germany.
  • Lewis SE; Genomics Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA, 94720, USA.
  • Robinson PN; Computational Biology Group, Institute for Medical Genetics and Human Genetics, Universitatsklinikum Charité, Augustenburger Platz 1, 13353, Berlin, Germany.
  • Smedley D; Skarnes Faculty Group, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK. ds5@sanger.ac.uk.
Mamm Genome ; 26(9-10): 548-55, 2015 Oct.
Article em En | MEDLINE | ID: mdl-26092691
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bases de Dados Genéticas / Doenças Genéticas Inatas Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Mamm Genome Assunto da revista: GENETICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bases de Dados Genéticas / Doenças Genéticas Inatas Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Mamm Genome Assunto da revista: GENETICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos