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Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features.
Pavlicek J, Soucek O, Vrtel R, Klaskova E, Hana V, Stara V, Adamova K, Fürst T, Hana V Jr, Kapralova S, Prochazka M, Snajderova M, Tomaskova H, Tüdös Z, Vrbicka D, Vrtel P, Zapletalova J, Tauber Z, Lebl J. Pavlicek J, et al. Among authors: vrtel r. Horm Res Paediatr. 2022;95(5):465-475. doi: 10.1159/000525823. Epub 2022 Jul 1. Horm Res Paediatr. 2022. PMID: 35970147
Fetal heart rhabdomyomatosis: a single-center experience.
Pavlicek J, Klaskova E, Kapralova S, Prochazka M, Vrtel R, Gruszka T, Kacerovsky M. Pavlicek J, et al. Among authors: vrtel r. J Matern Fetal Neonatal Med. 2021 Mar;34(5):701-707. doi: 10.1080/14767058.2019.1613365. Epub 2019 May 15. J Matern Fetal Neonatal Med. 2021. PMID: 31032681 Free article.
Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms.
Vrtel P, Vrtel R, Klaskova E, Vrbicka D, Adamova K, Pavlicek J, Hana V, Hana V, Soucek O, Stara V, Lebl J, Snajdrova M, Zapletalova J, Furst T, Kapralova S, Tauber Z, Krejcirikova E, Routilova M, Stellmachova J, Vodicka R, Prochazka M. Vrtel P, et al. Among authors: vrtel r. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022 Mar;166(1):63-67. doi: 10.5507/bp.2020.060. Epub 2021 Jan 12. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022. PMID: 33463629 Free article.
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. Spurná Z, et al. Among authors: vrtel r. Gene. 2024 Jan 20;892:147881. doi: 10.1016/j.gene.2023.147881. Epub 2023 Oct 6. Gene. 2024. PMID: 37806643 Free article.
[Analysis of free foetal DNA in maternal plasma using STR loci].
Vodicka R, Vrtel R, Procházka M, Santavá A, Dusek L, Vrbická D, Singh R, Krejciríková E, Schneiderová E, Santavý J. Vodicka R, et al. Among authors: vrtel r. Cas Lek Cesk. 2006;145(2):133-7. Cas Lek Cesk. 2006. PMID: 16521403 Czech.
66 results