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  • The Mitochondrial Disease Sequence Data Resource (MSeqDR) is a centralized genome and phenome bioinformatics resource built by the mitochondrial disease community to facilitate clinical diagnosis and research investigations of individual patient phenotypes, genomes, genes, and variants. It integrates community knowledge from expert‐curated databases with genomic and phenotype data shared by clinicians and researchers.

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  • This site provides access to the research output of the institution. Interface is available in English and Norwegian, most of the content is in Norwegian.

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  • This is an institutional repository for Erasmus Universiteit Rotterdam, providing access to the research output of the institution. The interface is available in English. Approximately half of items are not available as open access texts.

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  • International Dystrophic Epidermolysis Bullosa Patient Registry (DEB Register) provides phenotypic and genotypic information on DEB and the related COL7A1 mutations. The registry is intended to aid in disease diagnosis, genetic counseling, and discovery of novel insights.

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  • The Europeana website provides cultural heritage enthusiasts, professionals, teachers, and researchers with access to Europe's digital cultural heritage.

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1,649 Data sources
  • The Mitochondrial Disease Sequence Data Resource (MSeqDR) is a centralized genome and phenome bioinformatics resource built by the mitochondrial disease community to facilitate clinical diagnosis and research investigations of individual patient phenotypes, genomes, genes, and variants. It integrates community knowledge from expert‐curated databases with genomic and phenotype data shared by clinicians and researchers.

    more_vert
  • more_vert
  • more_vert
  • more_vert
  • This site provides access to the research output of the institution. Interface is available in English and Norwegian, most of the content is in Norwegian.

    more_vert
  • more_vert
  • This is an institutional repository for Erasmus Universiteit Rotterdam, providing access to the research output of the institution. The interface is available in English. Approximately half of items are not available as open access texts.

    more_vert
  • International Dystrophic Epidermolysis Bullosa Patient Registry (DEB Register) provides phenotypic and genotypic information on DEB and the related COL7A1 mutations. The registry is intended to aid in disease diagnosis, genetic counseling, and discovery of novel insights.

    more_vert
  • more_vert
  • The Europeana website provides cultural heritage enthusiasts, professionals, teachers, and researchers with access to Europe's digital cultural heritage.

    more_vert
  • chevron_left
  • 2
  • 3
  • 4
  • 5
  • 6
  • chevron_right