Concurrent Hearing and Genetic Screening among Newborns in Ningbo, China

OBJECTIVE: To detect the carrier rates of deafness gene variants in populations in Ningbo and analyze the risk of hereditary hearing loss through concurrent hearing and genetic screening tests. METHODS: Two thousand one hundred and seventy-four newborns were enrolled from November 2018 to August 201...

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Detalles Bibliográficos
Autores principales: Guomei, Cao, Luyan, Zhang, Lingling, Dai, Chunhong, Huang, Shan, Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8763501/
https://www.ncbi.nlm.nih.gov/pubmed/35047053
http://dx.doi.org/10.1155/2022/1713337

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8763501/
https://www.ncbi.nlm.nih.gov/pubmed/35047053
http://dx.doi.org/10.1155/2022/1713337

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