Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference33 articles.
1. Morton CC, Nance WE. Newborn hearing screening—a silent revolution. N Engl J Med. 2006;354:2151–64.
2. Shearer AE, Hildebrand MS, Smith RJH. Hereditary hearing loss and deafness overview. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, et al., editors. GeneReviews. Seattle (WA): University of Washington; 1993-2019.
3. Smith RJ, Bale JF Jr, White KR. Sensorineural hearing loss in children. Lancet. 2005;365:879–90.
4. Denoyelle F, Marlin S, Weil D, Moatti L, Chauvin P, Garabédian EN, et al. Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling. Lancet. 1999;353:1298–303.
5. Friedman TB, Griffith AJ. Human nonsyndromic sensorineural deafness. Annu Rev Genom Hum Genet. 2003;4:341–402.
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