Original Investigation

Analysis of GJB2 (Connexin 26) Mutation in Patients with Congenital Non-Syndromic Sensorineural Hearing Loss
  • Emin Kaskalan
  • Ebru Etem Önalan
  • İrfan Kaygusuz
  • Turgut Karlıdağ
  • Erol Keleş
  • Abdulvahap Akyiğit
  • Şinasi Yalçın
Turk Arch Otorhinolaryngol 2014; 52: 1-6 DOI: 10.5152/tao.2014.277
First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss
  • Berk Özyılmaz
  • Gül Caner Mercan
  • Özgür Kırbıyık
  • Taha Reşid Özdemir
  • Samira Özkara
  • Özge Özer Kaya
  • Yaşar Bekir Kutbay
  • Kadri Murat Erdoğan
  • Merve Saka Güvenç
  • Altuğ Koç
Turk Arch Otorhinolaryngol 2019; 57: 140-148 DOI: 10.5152/tao.2019.4320