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...

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Detalles Bibliográficos
Autores principales: Tang, Xiangrong, Liu, Lihua, Liang, Sulan, Liang, Meie, Liao, Tao, Luo, Shiqiang, Yan, Tizhen, Chen, Jianping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
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

Internet

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

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