Juan Domínguez-Aburto

Unique spectrum of GJB2 mutations in Mexico.

M. Tekin, E. Hernández-Zamora, Paulina Murphy-Ruiz, 2012, International journal of pediatric otorhinolaryngology.

Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort.

M. Tekin, S. Blanton, F. B. Cengiz, 2017, International journal of pediatric otorhinolaryngology.

Comprehensive Analysis via Exome Sequencing Uncovers Genetic Etiology in Autosomal Recessive Non-Syndromic Deafness in a Large Multiethnic Cohort

M. Tekin, S. Blanton, Shengru Guo, 2015, Genetics in Medicine.