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See Latest ArticlesGenotype-Phenotype Correlation for DFNA22: Characterization of Non-Syndromic, Autosomal Dominant, Progressive Sensorineural Hearing Loss due to MYO6 Mutations
Audiology & Neuro-Otology, 11/05/09
Topsakal V et al. – This study describes the phenotype of 2 Belgian families with SNHL linked to DFNA22, both with a pathogenic change in the deafness gene MYO6. The phenotypes of all hitherto reported DFNA22 families with mutations in the MYO6 gene have been studied and compared. It seems that genetic defects that spare the motor domain of the myosin VI protein have a milder phenotype.
Today in Basic Science/Genetics...keeping you current
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Pediatric cholesteatoma and variants in the gene encoding connexin 26
The Laryngoscope, 11/03/09
Audit of frequent attendees to an ENT emergency clinic
The Journal of Laryngology & Otology, 11/03/09
The nature of fibrous dysplasia
Head & Face Medicine, 11/10/09
Today in Otology/Neurotology...keeping you current
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Role of adenoids and adenoiditis in children with allergy and otitis media
Current Allergy and Asthma Reports, 10/22/09
Nystagmus during Attacks of Vestibular Migraine: An Aid in Diagnosis
Audiology & Neuro-Otology, 11/05/09
Hearing outcomes of daily intratympanic dexamethasone alone as a primary treatment modality for ISSHL
Otolaryngology Head and Neck Surgery, 10/28/09
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