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Concurrent Newborn Hearing and Genetic Screening in a Multi-Ethnic Population in South China
Hearing loss is a common sensory deficit in humans with intricate genomic landscape and mutational signature. Approximately 1–3 out of 1,000 newborns have hearing loss and up to 60% of these cases have a genetic etiology. In this study, we conducted the concurrent newborn hearing and genetic screeni...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8669824/ https://www.ncbi.nlm.nih.gov/pubmed/34917556 http://dx.doi.org/10.3389/fped.2021.734300 |