Čejnová V - Search Results

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The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes-A Comprehensive Study of the GJB2/DFNB1 Region.

Safka Brozkova D, Uhrova Meszarosova A, Lassuthova P, Varga L, Staněk D, Borecká S, Laštůvková J, Čejnová V, Rašková D, Lhota F, Gašperíková D, Seeman P. Safka Brozkova D, et al. Among authors: cejnova v. Genes (Basel). 2021 May 1;12(5):684. doi: 10.3390/genes12050684. Genes (Basel). 2021. PMID: 34062854 Free PMC article.

Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing.

Safka Brozkova D, Poisson Marková S, Mészárosová AU, Jenčík J, Čejnová V, Čada Z, Laštůvková J, Rašková D, Seeman P. Safka Brozkova D, et al. Among authors: cejnova v. Clin Genet. 2020 Dec;98(6):548-554. doi: 10.1111/cge.13839. Epub 2020 Sep 27. Clin Genet. 2020. PMID: 32860223

Czech family confirms the new 1p36.13-1p36.12 microdeletion syndrome.

Seeman P, Čejnová V, Černá Š, Rennerová L, Trková M, Kofer J, Laštůvková J. Seeman P, et al. Among authors: cejnova v. Clin Genet. 2022 Sep;102(3):244-245. doi: 10.1111/cge.14175. Epub 2022 Jun 21. Clin Genet. 2022. PMID: 35726688

Description of diagnosis of 45,X/46,XY ovotesticular DSD.

Ren Š, Harmaš V, Stará M, Laštůvkováj, Čejnová V. Ren Š, et al. Among authors: cejnova v. Ceska Gynekol. 2020 Winter;85(4):259-262. Ceska Gynekol. 2020. PMID: 33562981 English.

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