Cracking the auditory genetic code: Part II. Syndromic hereditary hearing impairment***
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Published:2000-05
Issue:3
Volume:21
Page:437-451
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ISSN:0196-0709
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Container-title:American Journal of Otolaryngology
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language:en
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Short-container-title:American Journal of Otolaryngology
Author:
TSENG C,LALWANI A
Subject
Otorhinolaryngology
Cited by
8 articles.
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1. Case Report: Exome Sequencing Identified Variants in Three Candidate Genes From Two Families With Hearing Loss, Onychodystrophy, and Epilepsy;Frontiers in Genetics;2021-11-29
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3. Familial Alström syndrome: a rare cause of bilateral progressive hearing loss ✩✩Please cite this article as: Bahmad F Jr., Costa CS, Teixeira MS, Barros-Filho J, Viana LM, Marshall J. Familial Alström syndrome: a rare cause of bilateral progressive hearing loss. Braz J Otorhinolaryngol. 2014;99-104.,✩✩✩✩Study conducted at Faculdade de Ciências da Saúde, Universidade de Brasília, Brasília, DF, Brazil.;Brazilian Journal of Otorhinolaryngology;2014-03
4. Alström Syndrome: Progressive Deafness and Blindness;Annals of Otology, Rhinology & Laryngology;2007-04
5. The Genetics of Otosclerosis: Pedigree Studies and Linkage Analysis;Otosclerosis and Stapes Surgery;2007