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1,932 Data sources

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  • This site provides access to the digitised copies of the institutions collection as well as teaching material. The interface is in German, English, Italian and Serbian.

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  • NARCIS provides access to scientific information, including (open access) publications from the repositories of all the Dutch universities, KNAW, NWO and a number of research institutes, which is not referenced in other citation databases.

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  • University of Groningen institutional repository

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  • This site provides access to the research output of the institution, The interface is available in French or English.

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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. The interface is available in German and English.

    more_vert
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1,932 Data sources
  • more_vert
  • This site provides access to the digitised copies of the institutions collection as well as teaching material. The interface is in German, English, Italian and Serbian.

    more_vert
  • NARCIS provides access to scientific information, including (open access) publications from the repositories of all the Dutch universities, KNAW, NWO and a number of research institutes, which is not referenced in other citation databases.

    more_vert
  • more_vert
  • University of Groningen institutional repository

    more_vert
  • This site provides access to the research output of the institution, The interface is available in French or English.

    more_vert
  • more_vert
  • more_vert
  • 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
  • This site provides access to the research output of the institution. The interface is available in German and English.

    more_vert
  • chevron_left
  • 1
  • 2
  • 3
  • 4
  • 5
  • chevron_right