Showing 1 - 2 results of 2 for search 'Vladimira Vallova', query time: 0.02s Refine Results
  1. 1
    Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype

    Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype by Jan Smetana, Vladimira Vallova, Vladimira Vallova, Marketa Wayhelova, Marketa Wayhelova, Eva Hladilkova, Hana Filkova, Vera Horinova, Petr Broz, Aneta Mikulasova, Renata Gaillyova, Petr Kuglík, Petr Kuglík

    Published 2021-10-01
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    Article
  2. 2
    Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders

    Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders by Marketa Wayhelova, Vladimira Vallova, Petr Broz, Aneta Mikulasova, Jan Smetana, Hana Dynkova Filkova, Dominika Machackova, Kristina Handzusova, Renata Gaillyova, Petr Kuglik

    Published 2024-02-01
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    Article

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