Navigating genetic diagnostics in patients with hearing loss
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Pediatrics, Perinatology, and Child Health
Reference56 articles.
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3. American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss;Alford;Genet Med,2014
4. EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss;Dahmani;Orphanet J Rare Dis,2015
5. HOMER2, a stereociliary scaffolding protein, is essential for normal hearing in humans and mice;Azaiez;PLoS Genet,2015
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