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Development of in‐house genetic screening for pediatric hearing loss
OBJECTIVES: To evaluate the efficiency of in‐house genetic testing for mutations causing the most common types of inherited, nonsyndromic, sensorineural hearing loss (SNHL). METHODS: Retrospective cohort study of 200 patients at a single, pediatric medical center with suspected or confirmed hearing...
Autores principales: | Doerfer, Karl W., Sander, Tara, Konduri, Girija G., Friedland, David R., Kerschner, Joseph E., Runge, Christina L. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314470/ https://www.ncbi.nlm.nih.gov/pubmed/32596493 http://dx.doi.org/10.1002/lio2.379 |
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