Genetic testing for congenital non-syndromic sensorineural hearing loss
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference41 articles.
1. American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss;Alford;Genet. Med.,2014
2. Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study;Del Castillo;Am. J. Hum. Genet.,2003
3. Genetic epidemiological studies of early-onset deafness in the U.S. school-age population;Marazita;Am. J. Med. Genet.,1993
4. Newborn hearing screening—a silent revolution;Morton;N. Engl. J. Med.,2006
5. Sensorineural hearing loss in children;Smith;Lancet,2005
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