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See Latest ArticlesHigh frequency of connexin26 (GJB2) mutations associated with nonsyndromic hearing loss in the population of Kerala, India
International Journal of Pediatric Otorhinolaryngology , 02/18/09
Joseph AY et al. - Mutations in connexin26 is responsible for 36% of non-syndromic sensorineural deafness in the population of Kerala, India.
Today in Basic Science/Genetics...keeping you current
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Study on TP53 Codon 72 Polymorphisms with Oral Carcinoma Susceptibility
Archives of Medical Research, 12/18/09
Role of the otolaryngologist in the treatment of struma ovarii
The Laryngoscope, 12/16/09
Association of the tumor necrosis factor-alpha -308 G/A polymorphism with nasal polyposis
European Archives of Oto-Rhino-Laryngology, 12/16/09
Today in Otology/Neurotology...keeping you current
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Patterns of hearing loss in tympanic membrane perforation resulting from physical blow to the ear: a prospective controlled cohort study
Clinical Otolaryngology, 12/18/09
Tympanometric values in young Malay adults: preliminary data
Singapore Medical Journal, 12/17/09
Three-Dimensional Computed Tomography Imaging of the Eustachian Tube Lumen in Patients with Patulous Eustachian Tube
Journal for Oto-Rhino-Laryngology, 12/17/09
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