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Publications by Tímea Tóth

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

Molecular Medicine
Molecular MedicineGeneticsMolecular Biology
2002English

Related publications

Y-Linked Inheritance of Non-Syndromic Hearing Impairment in a Large Chinese Family

Journal of Medical Genetics
Genetics
2004English

A Novel Biallelic Splice Site Mutation of TECTA Causes Moderate to Severe Hearing Impairment in an Algerian Family

International Journal of Pediatric Otorhinolaryngology
MedicineOtorhinolaryngologyPediatricsPerinatologyChild Health
2016English

Second Family With Hearing Impairment Linked to 19q13 and Refined DFNA4 Localisation

European Journal of Human Genetics
Genetics
2002English

A Point Mutation in the Gene for Asparagine-Linked Glycosylation 10B (Alg10b) Causes Nonsyndromic Hearing Impairment in Mice (Mus Musculus)

PLoS ONE
Multidisciplinary
2013English

Phenotypic Characterization of Hereditary Hearing Impairment Linked to DFNA25

Archives of Otolaryngology–Head & Neck Surgery
2003English

A Dutch Family With Hearing Loss Linked to the DFNA20/26 Locus

Archives of Otolaryngology–Head & Neck Surgery
2004English

Genetic Basis of Y-Linked Hearing Impairment

American Journal of Human Genetics
Genetics
2013English

A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family

BioMed Research International
ImmunologyMolecular BiologyBiochemistryMicrobiology MedicineGenetics
2018English

Causes of H Earing Impairment in Our Region: A Sadarem Project Report

Journal of Evolution of Medical and Dental Sciences
2015English

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