The genetics of deafness
Author:
Publisher
Wiley
Subject
Genetics (clinical),Neuropsychology and Physiological Psychology,Pediatrics, Perinatology and Child Health
Reference55 articles.
1. A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family
2. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss
3. Fine Mapping of the Human Biotinidase Gene and Haplotype Analysis of Five Common Mutations
4. Usher syndrome: Definition and estimate of prevalence from two high-risk populations
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