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

Case Report

Mondini and Michel deformities of the inner ear: a case report
  • Çağlar Çallı
  • Ercan Pınar
  • Semih Öncel
  • A. Kadir İmre
  • Melda Apaydın
Turk Arch Otorhinolaryngol 2010; 48: 37-41 DOI: 10.2399/tao.06.027