Genetic testing for pediatric hearing loss: no time to waste
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/s00439-021-02333-9.pdf
Reference17 articles.
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2. Billings KR, Kenna MA (1999) Causes of pediatric sensorineural hearing loss: yesterday and today. Arch Otolaryngol Head Neck Surg 125(5):517–521
3. Boudewyns A, Declau F, van den Ende J, Hofkens A, Dirckx S, Van de Heyning P (2016) Auditory neuropathy spectrum disorder (ANSD) in referrals from neonatal hearing screening at a well-baby clinic. Eur J Pediatr 175(7):993–1000. https://doi.org/10.1007/s00431-016-2735-5 (PMID: 27220871)
4. Chan DK, Chang KW (2014) GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype. Laryngoscope 124(2):E34-53. https://doi.org/10.1002/lary.24332 (PMID: 23900770)
5. Fowler KB, McCollister FP, Sabo DL, Shoup AG, Owen KE, Woodruff JL, Cox E, Mohamed LS, Choo DI, Boppana SB, CHIMES Study (2017) A targeted approach for congenital cytomegalovirus screening within newborn hearing screening. Pediatrics 139(2):e20162128. https://doi.org/10.1542/peds.2016-2128 (PMID: 28049114; PMCID: PMC5260148)
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