Diagnostic efficacy and clinical utility of whole-exome sequencing in Czech pediatric patients with rare and undiagnosed diseases by Katerina Slaba, Petra Pokorna, Robin Jugas, Hana Palova, Dagmar Prochazkova, Stefania Aulicka, Klara Spanelova, Pavlina Danhofer, Ondrej Horak, Jana Tuckova, Petra Kleiblova, Renata Gaillyova, Matej Hrunka, Martin Jouza, Blanka Pinkova, Jan Papez, Petra Konecna, Jana Zidkova, Petr Stourac, Jaroslav Sterba, Regina Demlova, Eva Demlova, Petr Jabandziev, Ondrej Slaby

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