Associated Papers
Prevalence of DFNB1 mutations in Slovak patients with non-syndromic hearing loss.
Minárik G et al.
International Journal of Pediatric Otorhinolaryngology, 2012
High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL).
Minárik G et al.
General Physiology and Biophysics, 2003
Select a paper to view details