In Reference toTemporal Bone Imaging inGJB2Deafness
Author:
Publisher
Wiley
Subject
Otorhinolaryngology
Reference9 articles.
1. Temporal bone imaging in GJB2 deafness;Propst;Laryngoscope,2006
2. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.;Green;JAMA,1999
3. Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1).;Cohn;Pediatrics,1999
4. Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.;Denoyelle;Lancet,1999
5. Outcomes of clinical examination and genetic testing of 500 individuals with hearing loss evaluated through a genetics of hearing loss clinic.;Yaeger;Am J Med Genet A,2006
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2. Acueducto vestibular dilatado como causa de hipoacusia postneonatal;Acta Otorrinolaringológica Española;2023-12
3. Genetic Screening for 35delG Mutation in Egyptian Patients with Profound Sensorineural Hearing Loss Scheduled for Cochlear Implantation: A Population-Based Study;ORL;2021
4. Enlarged vestibular aqueduct and Mondini Malformation: audiological, clinical, radiologic and genetic features;European Archives of Oto-Rhino-Laryngology;2020-09-10
5. DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes;Frontiers in Molecular Neuroscience;2017-12-22
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