Search Results - Zunova, Hana

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  1. 1
    Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease

    Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease by Neřoldová, Magdaléna, Ciara, Elżbieta, Slatinská, Janka, Fraňková, Soňa, Lišková, Petra, Kotalová, Radana, Globinovská, Janka, Šafaříková, Markéta, Pfeiferová, Lucie, Zůnová, Hana, Mrázová, Lenka, Stránecký, Viktor, Vrbacká, Alena, Fabián, Ondřej, Sticová, Eva, Skanderová, Daniela, Šperl, Jan, Kalousová, Marta, Zima, Tomáš, Macek, Milan, Pawlowska, Joanna, Knisely, A S, Kmoch, Stanislav, Jirsa, Milan

    Published in PloS one
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  2. 2
    A unique coincidence of a 17q12 deletion and duplication in a Czech family led to a refined genotype–phenotype correlation

    A unique coincidence of a 17q12 deletion and duplication in a Czech family led to a refined genotype–phenotype correlation by Zunova, Hana, Stolfa, Miroslav, Kunikova, Tereza, Novotna, Drahuse, Valkovicova, Radka, Štěrbová, Katalin, Vlckova, Marketa

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  3. 3
    Genetic testing in children enrolled in epilepsy surgery program. A real-life study

    Genetic testing in children enrolled in epilepsy surgery program. A real-life study by Straka, Barbora, Splitkova, Barbora, Vlckova, Marketa, Tesner, Pavel, Rezacova, Hana, Krskova, Lenka, Koblizek, Miroslav, Kyncl, Martin, Maulisova, Alice, Bukacova, Katerina, Uhrova-Meszarosova, Anna, Musilova, Alena, Kudr, Martin, Ebel, Matyas, Belohlavkova, Anezka, Jahodova, Alena, Liby, Petr, Tichy, Michal, Jezdik, Petr, Zamecnik, Josef, Aronica, Eleonora, Krsek, Pavel

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    Genetic Testing for Malformations of Cortical Development: A Clinical Diagnostic Study

    Genetic Testing for Malformations of Cortical Development: A Clinical Diagnostic Study by Straka, Barbora, Hermanovska, Barbora, Krskova, Lenka, Zamecnik, Josef, Vlckova, Marketa, Balascakova, Miroslava, Tesner, Pavel, Jezdik, Petr, Tichy, Michal, Kyncl, Martin, Musilova, Alena, Lassuthova, Petra, Marusic, Petr, Krsek, Pavel

    Published in Neurology. Genetics
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  5. 5
    A unique coincidence of a 17q12 deletion and duplication in a Czech family led to a refined genotype-phenotype correlation

    A unique coincidence of a 17q12 deletion and duplication in a Czech family led to a refined genotype-phenotype correlation by Zunova, Hana, Stolfa, Miroslav, Kunikova, Tereza, Novotna, Drahuse, Valkovicova, Radka, Štěrbová, Katalin, Vlckova, Marketa

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