Jana Laštůvková

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 sequencing

Dana Šafka Brožková, Simona Poisson Marková, Anna Uhrová Mészárosová et al. · Clinical Genetics · 2020 · 33 citations

Life Sciences, Genetics, Molecular Genetics +16

DFNB49 is an important cause of non‐syndromic deafness in Czech Roma patients but not in the general Czech population

Dana Šafka Brožková, Jana Laštůvková, Hana Štěpánková et al. · Clinical Genetics · 2011 · 24 citations

Life Sciences, Genetics, Molecular Genetics +17

Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene

Zdeněk Čada, Dana Šafka Brožková, Zuzana Balatková et al. · European Archives of Oto-Rhino-Laryngology · 2019 · 21 citations

Life Sciences, Genetics, Molecular Genetics +11

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

Dana Šafka Brožková, Anna Uhrová Mészárosová, Petra Laššuthová et al. · Genes · 2021 · 18 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Fatal neonatal nephrocutaneous syndrome in 18 Roma children with <i>EGFR</i> deficiency

Stella Mazurová, Markéta Tesařová, J Zeman et al. · The Journal of Dermatology · 2020 · 14 citations

Medicine, Genetics, Pediatrics +17