Spectrum and frequencies of non <scp> <i>GJB2</i> </scp> gene mutations in Czech patients with early non‐syndromic hearing loss detected by gene panel NGS and whole‐exome sequencingDana Šafka Brožková, Pavel Seeman, Simona Poisson Marková et al.|Clinical Genetics|2020Cited by 35
<i>STRC</i> Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech PopulationSimona Poisson Marková, Pavel Seeman, Anna Uhrová Mészárosová et al.|Genetic Testing and Molecular Biomarkers|2018Cited by 26
Mutations in eight small DFNB genes are not a frequent cause of non-syndromic hereditary hearing loss in Czech patientsSimona Poisson Marková, Pavel Seeman, Dana Šafka Brožková et al.|International Journal of Pediatric Otorhinolaryngology|2016Cited by 17
Author response for "Spectrum and frequencies of non <scp> <i>GJB2</i> </scp> gene mutations in Czech patients with early non‐syndromic hearing loss detected by <scp>NGS</scp> gene panel and <scp>WES</scp>"Dana Šafka Brožková, Pavel Seeman, Simona Poisson Marková et al.|Unknown|2020Cited by 0
Author response for "Spectrum and frequencies of non <scp> <i>GJB2</i> </scp> gene mutations in Czech patients with early non‐syndromic hearing loss detected by <scp>NGS</scp> gene panel and <scp>WES</scp>"Dana Šafka Brožková, Pavel Seeman, Simona Poisson Marková et al.|Unknown|2020Cited by 0