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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 1
2003 2
2004 2
2006 4
2007 2
2008 1
2009 2
2010 6
2011 2
2012 1
2013 5
2014 1
2015 3
2016 1
2017 4
2018 5
2019 7
2020 3
2021 2
2022 3
2023 2
2024 1

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56 results

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Page 1
Genetic findings in Czech patients with limb girdle muscular dystrophy.
Zídková J, Kramářová T, Kopčilová J, Réblová K, Haberlová J, Mazanec R, Voháňka S, Gřegořová A, Langová M, Honzík T, Šoukalová J, Ošlejšková H, Solařová P, Vyhnálková E, Fajkusová L. Zídková J, et al. Among authors: reblova k. Clin Genet. 2023 Nov;104(5):542-553. doi: 10.1111/cge.14407. Epub 2023 Aug 1. Clin Genet. 2023. PMID: 37526466
Importance of base-pair opening for mismatch recognition.
Bouchal T, Durník I, Illík V, Réblová K, Kulhánek P. Bouchal T, et al. Among authors: reblova k. Nucleic Acids Res. 2020 Nov 18;48(20):11322-11334. doi: 10.1093/nar/gkaa896. Nucleic Acids Res. 2020. PMID: 33080020 Free PMC article.
Next-generation sequencing in children with epilepsy: The importance of precise genotype-phenotype correlation.
Horák O, Burešová M, Kolář S, Španělová K, Jeřábková B, Gaillyová R, Česká K, Réblová K, Šoukalová J, Zídková J, Fajkusová L, Ošlejšková H, Rektor I, Danhofer P. Horák O, et al. Among authors: reblova k. Epilepsy Behav. 2022 Mar;128:108564. doi: 10.1016/j.yebeh.2022.108564. Epub 2022 Jan 19. Epilepsy Behav. 2022. PMID: 35065395
Bending of DNA duplexes with mutation motifs.
Růžička M, Souček P, Kulhánek P, Radová L, Fajkusová L, Réblová K. Růžička M, et al. Among authors: reblova k. DNA Res. 2019 Aug 1;26(4):341-352. doi: 10.1093/dnares/dsz013. DNA Res. 2019. PMID: 31230075 Free PMC article.
Inherited ichthyoses: molecular causes of the disease in Czech patients.
Borská R, Pinková B, Réblová K, Bučková H, Kopečková L, Němečková J, Puchmajerová A, Malíková M, Hermanová M, Fajkusová L. Borská R, et al. Among authors: reblova k. Orphanet J Rare Dis. 2019 May 2;14(1):92. doi: 10.1186/s13023-019-1076-7. Orphanet J Rare Dis. 2019. PMID: 31046801 Free PMC article.
A GP1BA Variant in a Czech Family with Monoallelic Bernard-Soulier Syndrome.
Skalníková M, Staňo Kozubík K, Trizuljak J, Vrzalová Z, Radová L, Réblová K, Holbová R, Kurucová T, Svozilová H, Štika J, Blaháková I, Dvořáčková B, Prudková M, Stehlíková O, Šmída M, Křen L, Smejkal P, Pospíšilová Š, Doubek M. Skalníková M, et al. Among authors: reblova k. Int J Mol Sci. 2022 Jan 14;23(2):885. doi: 10.3390/ijms23020885. Int J Mol Sci. 2022. PMID: 35055070 Free PMC article.
56 results