Clinical-genetic analysis of selected genes involved in the development of the human skeleton in 128 Czech patients with suspected congenital skeletal abnormalities
Spurná, Z, Čapková, P, Punová, L, DuchoslavovÁ, J, Aleksijevic, D, Venháčová, P, Srovnal, J, Štellmachová, J, Curtisová, V, Bitnerová, V, Petřková, J, Kolaříková, K, Janíková, M, Kratochvílová, R, Vrtěl, P, Vodička, R, Vrtěl, R, Zapletalová, J
Published in Gene (20.01.2024)
Published in Gene (20.01.2024)
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Prenatal detection of copy number variants in fetuses with detected congenital devolpmental disordes, from 2015 to 2020 by Multiplex Ligation-Dependent Probe Amplification and microarray analysis
Štefeková, Andrea, Čapková, Pavlína, Curtisová, Václava, Mracká, Enghjargalan, Filipová, Hana, Spurná, Zuzana, Procházka, Martin, Ľubušký, Marek, Pilka, Radovan, Vrtěl, Radek
Published in Ceská gynekologie (01.01.2023)
Published in Ceská gynekologie (01.01.2023)
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