Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China

To understand the possible carrier status of genes associated with hereditary hearing loss (HHL) in the general population among local residents and to give genetic counseling for pregnant women. A total of 3541 subjects were recruited. We used multiplex PCR technology combined with next-generation...

Descripción completa

Detalles Bibliográficos
Autores principales: Hu, Hua, Zhou, Peng, Wu, Jiayan, Lei, Wei, Wang, Yang, Yang, Ying, Liu, Hailiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084083/
https://www.ncbi.nlm.nih.gov/pubmed/33907123
http://dx.doi.org/10.1097/MD.0000000000025647

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084083/
https://www.ncbi.nlm.nih.gov/pubmed/33907123
http://dx.doi.org/10.1097/MD.0000000000025647

Ejemplares similares