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Stepwise molecular-genetic examination in aborted fetuses.
Trková Marie, Prokopcová Lenka, Bakardjieva-Mihaylova Violeta, Němec Michael, Borgulová Irena, Vilímová Zuzana, Dohnalová Lucie, Bečvářová Věra, Bittóová Martina, Horáček Jiří, Stejskal David, Koudová Monika. Trková Marie, et al. Among authors: stejskal david. Ceska Gynekol. 2022;87(2):104-110. doi: 10.48095/cccg2022104. Ceska Gynekol. 2022. PMID: 35667861 English.
[Implementation of arrays in first trimester prenatal diagnosis].
Trková M, Putzová M, Bečvářová V, Horáček J, Soldátová I, Krautová L, Sekowská M, Hodačová J, Hnyková L, Hlavová E, Smetanová D, Stejskal D. Trková M, et al. Ceska Gynekol. 2015 Jun;80(3):176-80. Ceska Gynekol. 2015. PMID: 26087211 Czech.
[Application of SNP array method in prenatal diagnosis].
Becvárová V, Hynek M, Putzová M, Soldátová I, Horácek J, Smetanová D, Kulovaný E, Matousková M, Krutílková V, Hlavová E, Rasková D, Hejtmánková M, Cutka K, Cutka D, Stejskal D, Mihalová R, Trková M. Becvárová V, et al. Ceska Gynekol. 2011 Sep;76(4):261-7. Ceska Gynekol. 2011. PMID: 22026066 Czech.
SNP array and phenotype correlation shows that FLI1 deletion per se is not responsible for thrombocytopenia development in Jacobsen syndrome.
Trkova M, Becvarova V, Hynek M, Hnykova L, Hlavova E, Kreckova G, Kulovany E, Cutka D, Zatloukalova J, Markova K, Sukova M, Horacek J, Stejskal D. Trkova M, et al. Among authors: stejskal d. Am J Med Genet A. 2012 Oct;158A(10):2545-50. doi: 10.1002/ajmg.a.35537. Epub 2012 Aug 7. Am J Med Genet A. 2012. PMID: 22887642
Expanded DMPK repeats in dizygotic twins referred for diagnosis of autism versus absence of expanded DMPK repeats at screening of 330 children with autism.
Musova Z, Hancarova M, Havlovicova M, Pourova R, Hrdlicka M, Kraus J, Trkova M, Stejskal D, Sedlacek Z. Musova Z, et al. Among authors: stejskal d. Neuropsychiatr Dis Treat. 2016 Sep 19;12:2367-2372. doi: 10.2147/NDT.S113917. eCollection 2016. Neuropsychiatr Dis Treat. 2016. PMID: 27695335 Free PMC article.
170 results