Diagnostic efficacy and clinical utility of whole-exome sequencing in Czech pediatric patients with rare and undiagnosed diseases.

Autor: Slaba, Katerina1 (AUTHOR) slaba.katerina@fnbrno.cz, Pokorna, Petra2,3 (AUTHOR), Jugas, Robin2,3 (AUTHOR), Palova, Hana2 (AUTHOR), Prochazkova, Dagmar1 (AUTHOR), Aulicka, Stefania4 (AUTHOR), Spanelova, Klara4 (AUTHOR), Danhofer, Pavlina4 (AUTHOR), Horak, Ondrej4 (AUTHOR), Tuckova, Jana1 (AUTHOR), Kleiblova, Petra5,6 (AUTHOR), Gaillyova, Renata7 (AUTHOR), Hrunka, Matej1 (AUTHOR), Jouza, Martin1 (AUTHOR), Pinkova, Blanka1 (AUTHOR), Papez, Jan1 (AUTHOR), Konecna, Petra1 (AUTHOR), Zidkova, Jana8 (AUTHOR), Stourac, Petr9,10 (AUTHOR), Sterba, Jaroslav11 (AUTHOR)
Zdroj: Scientific Reports. 11/20/2024, Vol. 14 Issue 1, p1-11. 11p.
Databáze: Academic Search Ultimate
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