Dagmar Ras̆ková

Spectrum and frequencies of mutations in the <i>GJB2</i> (<i>Cx26</i>) gene among 156 Czech patients with pre‐lingual deafness

Pavel Seeman, Marcela Malíková, Dagmar Ras̆ková et al. · Clinical Genetics · 2004 · 56 citations

Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2

Michael J. Dixon, Jill Dixon, Dagmar Ras̆ková et al. · Human Molecular Genetics · 1992 · 49 citations

Genetics, Genetic Epidemiology, Collins Syndrome +17

Spectrum and Frequency of <i>SLC26A4</i> Mutations Among Czech Patients with Early Hearing Loss with and without Enlarged Vestibular Aqueduct (EVA)

Radka Kremlíková Pourová, Petr Janoušek, Michal Jurovčík et al. · Annals of Human Genetics · 2010 · 40 citations

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 · 32 citations

Double Heterozygosity with Mutations Involving both the <i>GJB2</i> and <i>GJB6</i> Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population

Pavel Seeman, O. Bendová, Dagmar Ras̆ková et al. · Annals of Human Genetics · 2005 · 31 citations · Full text