Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference30 articles.
1. Morton CC, Nance WE. Newborn hearing screening-a silent revolution. N Engl J Med. 2006;354:2151–64.
2. Koffler T, Ushakov K, Avraham KB. Genetics of hearing loss: syndromic. Otolaryngol Clin North Am. 2015 ;48:1041–61.
3. Parker M, Bitner-Glindzicz M. Genetic investigations in childhood deafness. Arch Dis Child. 2014;0:1–8. http://www.ncbi.nlm.nih.gov/pubmed/25324569
4. Kimberling WJ, Hildebrand MS, Shearer AE, Jensen ML, Halder JA, Trzupek K, et al. Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children. Genet Med. 2010;12:512–6.
5. Jouret G, Poirsier C, Spodenkiewicz M, Jaquin C, Gouy E, Arndt C, et al. Genetics of Usher syndrome: new insights from a meta-analysis. Otol Neurotol. 2019;40:121–9.
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