Publications by authors named "Vlasta Cejnova"

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Czech family confirms the new 1p36.13-1p36.12 microdeletion syndrome.
Pavel Seeman, Vlasta Čejnová, Šárka Černá, Ladislava Rennerová, Marie Trková

Clin Genet· September 2022

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The Cause of Hereditary Hearing Loss in Heterozygotes-A Comprehensive Study of the /DFNB1 Region.
Dana Safka Brozkova, Anna Uhrova Meszarosova, Petra Lassuthova, Lukáš Varga, David Staněk

Genes (Basel)· May 2021

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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.
Dana Safka Brozkova, Simona Poisson Marková, Anna Uhrová Mészárosová, Ján Jenčík, Vlasta Čejnová

Clin Genet· December 2020

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