Showing 1 - 3 results of 3 for search 'Anja K Mayer', query time: 0.02s Refine Results
  1. 1
    Paternal Uniparental Isodisomy of Chromosome 2 in a Patient with <i>CNGA3</i>-Associated Autosomal Recessive Achromatopsia

    Paternal Uniparental Isodisomy of Chromosome 2 in a Patient with <i>CNGA3</i>-Associated Autosomal Recessive Achromatopsia by Susanne Kohl, Britta Baumann, Francesca Dassie, Anja K. Mayer, Maria Solaki, Peggy Reuter, Laura Kühlewein, Bernd Wissinger, Pietro Maffei

    Published 2021-07-01
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    Article
  2. 2
    CDHR1 mutations in retinal dystrophies

    CDHR1 mutations in retinal dystrophies by Katarina Stingl, Anja K. Mayer, Pablo Llavona, Lejla Mulahasanovic, Günther Rudolph, Samuel G. Jacobson, Eberhart Zrenner, Susanne Kohl, Bernd Wissinger, Nicole Weisschuh

    Published 2017-08-01
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    Article
  3. 3
    Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing.

    Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing. by Nicole Weisschuh, Anja K Mayer, Tim M Strom, Susanne Kohl, Nicola Glöckle, Max Schubach, Sten Andreasson, Antje Bernd, David G Birch, Christian P Hamel, John R Heckenlively, Samuel G Jacobson, Christina Kamme, Ulrich Kellner, Erdmute Kunstmann, Pietro Maffei, Charlotte M Reiff, Klaus Rohrschneider, Thomas Rosenberg, Günther Rudolph, Rita Vámos, Balázs Varsányi, Richard G Weleber, Bernd Wissinger

    Published 2016-01-01
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    Article

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