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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: srovnal j. PeerJ. 2019 Jan 9;6:e6183. doi: 10.7717/peerj.6183. eCollection 2019. PeerJ. 2019. PMID: 30647996 Free PMC article.
MLPA analysis of 32 foetuses with a congenital heart defect and 1 foetus with renal defects - pilot study. The significant frequency rate of presented pathological CNV.
Stefekova A, Capkova P, Capkova Z, Curtisova V, Srovnal J, Mracka E, Klaskova E, Prochazka M. Stefekova A, et al. Among authors: srovnal j. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022 May;166(2):187-194. doi: 10.5507/bp.2021.019. Epub 2021 Mar 31. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022. PMID: 33824538 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: srovnal j. Gene. 2024 Jan 20;892:147881. doi: 10.1016/j.gene.2023.147881. Epub 2023 Oct 6. Gene. 2024. PMID: 37806643 Free article.
Epithelial to mesenchymal transition and microRNA expression are associated with spindle and apocrine cell morphology in triple-negative breast cancer.
Koleckova M, Ehrmann J, Bouchal J, Janikova M, Brisudova A, Srovnal J, Staffova K, Svoboda M, Slaby O, Radova L, Vomackova K, Melichar B, Veverkova L, Kolar Z. Koleckova M, et al. Among authors: srovnal j. Sci Rep. 2021 Mar 4;11(1):5145. doi: 10.1038/s41598-021-84350-2. Sci Rep. 2021. PMID: 33664322 Free PMC article.
54 results