Search Results - Martina Škopková

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    Genetic testing is necessary for correct diagnosis and treatment in patients with isolated methylmalonic aciduria: a case report by Katarína Brennerová, Martina Škopková, Mária Ostrožlíková, Jana Šaligová, Juraj Staník, Vladimír Bzdúch, Daniela Gašperíková

    Published 2021
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    Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case report by Lukas Varga, Daniel Danis, Martina Skopkova, Ivica Masindova, Zuzana Slobodova, Lucia Demesova, Milan Profant, Daniela Gasperikova

    Published 2019
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