T. Tóth

Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene

M. Tekin, K. Arnos, A. Pandya, 2009, European Journal of Human Genetics.

GJB2 mutations in patients with non‐syndromic hearing loss from Northeastern Hungary

Nikolaus Blin, Markus Pfister, H. Zenner, 2004, Human mutation.

GJB2 mutations and degree of hearing loss: a multicenter study.

Mustafa Tekin, Umberto Ambrosetti, Nikolaus Blin, 2005, American journal of human genetics.

Phenotypic characterization of a DFNA6 family showing progressive low-frequency sensorineural hearing impairment.

H. Zenner, M. Pfister, I. Sziklai, 2006, International journal of pediatric otorhinolaryngology.

Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations

C. Cremers, W. Reardon, H. Kremer, 2002, Human Genetics.

A 4bp-Insertion in the eya-Homologous Region (eyaHR) of EYA4 Causes Hearing Impairment in a Hungarian Family Linked to DFNA10

P. Nürnberg, H. Zenner, N. Blin, 2002, Molecular medicine.

Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients

H. Zenner, N. Blin, W. Szyfter, 2002, Human mutation.

Coincidence of mutations in different connexin genes in Hungarian patients.

N. Blin, M. Pfister, S. Kupka, 2007, International journal of molecular medicine.

A new mutation in the human pres gene and its effect on prestin function.

Jing Zheng, L. Muszbek, I. Sziklai, 2007, International journal of molecular medicine.