Showing 1 - 2 results of 2 for search 'Björn Reusch', query time: 0.01s Refine Results
  1. 1
    Severe Joubert syndrome in family with homozygous POC1B p.Arg106Pro variant is due to a co-inherited deep-intronic mutation in the neighboring CEP290 gene

    Severe Joubert syndrome in family with homozygous POC1B p.Arg106Pro variant is due to a co-inherited deep-intronic mutation in the neighboring CEP290 gene by Christian Betz, Björn Reusch, Thomas Langmann, Sandra Habbig, Bodo B. Beck, Hanno J. Bolz

    Published 2025-07-01
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  2. 2
    Effective Newborn Screening for Type 1 and 3 Primary Hyperoxaluria

    Effective Newborn Screening for Type 1 and 3 Primary Hyperoxaluria by Bernd Hoppe, Cristina Martin-Higueras, Lodovica Borghese, Sophie Kaspar, Björn Reusch, Bodo B. Beck, Adam Walli, Ella Janzen, Sebastian Hegert, Nils Janzen, Katharina Hohenfellner

    Published 2025-01-01
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