The qualitative experiences of otolaryngologists with genetic services in pediatric hearing loss evaluation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Public Health, Environmental and Occupational Health,Epidemiology
Link
https://link.springer.com/content/pdf/10.1007/s12687-023-00649-9.pdf
Reference27 articles.
1. Alford RL, Arnos KS, Fox M, Lin JW, Palmer CG, Pandya A, Rehm HL, Robin NH, Scott DA, Yoshinaga-Itano C, ACMG Working Group on Update of Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss, & Professional Practice and Guidelines Committee (2014) American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. Genet Med 16(4):347–355. https://doi.org/10.1038/gim.2014.2
2. Bajguz D, Danylchuk NR, Czarniecki M, Selig JP, Sutphen R, Kaylor J. Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans [published online ahead of print, 2021 Dec 23]. J Genet Couns. 2021;https://doi.org/10.1002/jgc4.1543. https://doi.org/10.1002/jgc4.1543
3. Brunger JW, Murray GS, O’Riordan M, Matthews AL, Smith RJ, Robin NH (2000) Parental attitudes toward genetic testing for pediatric deafness. Am J Hum Genet 67(6):1621–1625. https://doi.org/10.1086/316901
4. Casazza G, Meier JD (2017) Evaluation and management of syndromic congenital hearing loss. Curr Opin Otolaryngol Head Neck Surg 25(5):378–384. https://doi.org/10.1097/MOO.0000000000000397
5. Duncan RD, Prucka S, Wiatrak BJ, Smith RJ, Robin NH (2007) Pediatric otolaryngologists’ use of genetic testing. Arch Otolaryngol Head Neck Surg. 133(3):231–236. https://doi.org/10.1001/archotol.133.3.231
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