Molecular investigation in children candidates and submitted to cochlear implantation
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology
Reference19 articles.
1. The effect of GJB2 allele variants on performance after cochlear implantation;Bauer;Laryngoscope,2003
2. Clinical studies of families with hearing loss attributable to mutations in the connexin gene (GJB2/DFNB1);Cohn;Pedriatric,1999
3. Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss;Cohn;Am J Med Genet,1999
4. Performance of coclear implant recipients with GJB2-related deafness;Green;Am J Med Genet,2002
5. Kenna MA, Wu BL, Cotanche DA, Korf BR, Rehm HL. Connexin 26 studies in patients with sensorineural hearing loss. Arch Otolaryngol Head Neck Surg 127:1037-42.
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5. Targeted Resequencing of Deafness Genes Reveals a FounderMYO15AVariant in Northeastern Brazil;Annals of Human Genetics;2016-11
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