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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: cutka 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
[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. Among authors: cutka d. Ceska Gynekol. 2011 Sep;76(4):261-7. Ceska Gynekol. 2011. PMID: 22026066 Czech.
Pregnancy Termination and Postnatal Major Congenital Heart Defect Prevalence After Introduction of Prenatal Cardiac Screening.
Tomek V, Jicínská H, Pavlícek J, Kovanda J, Jehlicka P, Klásková E, Mrázek J, Cutka D, Smetanová D, Brešták M, Vlašín P, Pavlíková M, Chaloupecký V, Janoušek J, Marek J. Tomek V, et al. Among authors: cutka d. JAMA Netw Open. 2023 Sep 5;6(9):e2334069. doi: 10.1001/jamanetworkopen.2023.34069. JAMA Netw Open. 2023. PMID: 37713196 Free PMC article.