Showing 1 - 3 results of 3 for search 'Julia Stellmachova', query time: 0.03s Refine Results
  1. 1
    Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development

    Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development by Kristyna Kolarikova, Radek Vodicka, Radek Vrtel, Julia Stellmachova, Martin Prochazka, Katerina Mensikova, Petr Kanovsky

    Published 2022-03-01
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  2. 2
    High-Throughput Sequencing Haplotype Analysis Indicates in <i>LRRK2</i> Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic

    High-Throughput Sequencing Haplotype Analysis Indicates in <i>LRRK2</i> Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic by Kristyna Kolarikova, Radek Vodicka, Radek Vrtel, Julia Stellmachova, Martin Prochazka, Katerina Mensikova, Tereza Bartonikova, Tomas Furst, Petr Kanovsky, Jan Geryk

    Published 2022-01-01
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  3. 3
    Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing

    Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing by Petr Vrtel, Ludek Slavik, Radek Vodicka, Julia Stellmachova, Martin Prochazka, Jana Prochazkova, Jana Ulehlova, Peter Rohon, Tomas Simurda, Jan Stasko, Ivana Martinkova, Radek Vrtel

    Published 2022-04-01
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