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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: becvarova vera. 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: becvarova v. 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
MLPA is a practical and complementary alternative to CMA for diagnostic testing in patients with autism spectrum disorders and identifying new candidate CNVs associated with autism.
Capkova P, Srovnal J, Capkova Z, Staffova K, Becvarova V, Trkova M, Adamova K, Santava A, Curtisova V, Hajduch M, Prochazka M. Capkova P, et al. Among authors: becvarova v. PeerJ. 2019 Jan 9;6:e6183. doi: 10.7717/peerj.6183. eCollection 2019. PeerJ. 2019. PMID: 30647996 Free PMC article.
19 results