Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China

Concurrent hearing and genetic screening of newborns is expected to play important roles not only in early detection and diagnosis of congenital deafness, which triggers intervention, but also in predicting late-onset and progressive hearing loss and identifying individuals who are at risk of drug-i...

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Detalhes bibliográficos
Publicado no:Am J Hum Genet
Main Authors: Dai, Pu, Huang, Li-Hui, Wang, Guo-Jian, Gao, Xue, Qu, Chun-Yan, Chen, Xiao-Wei, Ma, Fu-Rong, Zhang, Jie, Xing, Wan-Li, Xi, Shu-Yan, Ma, Bin-Rong, Pan, Ying, Cheng, Xiao-Hua, Duan, Hong, Yuan, Yong-Yi, Zhao, Li-Ping, Chang, Liang, Gao, Ru-Zhen, Liu, Hai-Hong, Zhang, Wei, Huang, Sha-Sha, Kang, Dong-Yang, Liang, Wei, Zhang, Ke, Jiang, Hong, Guo, Yong-Li, Zhou, Yi, Zhang, Wan-Xia, Lyu, Fan, Jin, Ying-Nan, Zhou, Zhen, Lu, Hong-Li, Zhang, Xin, Liu, Ping, Ke, Jia, Hao, Jin-Sheng, Huang, Hai-Meng, Jiang, Di, Ni, Xin, Long, Mo, Zhang, Luo, Qiao, Jie, Morton, Cynthia Casson, Liu, Xue-Zhong, Cheng, Jing, Han, De-Min
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6817518/
https://ncbi.nlm.nih.gov/pubmed/31564438
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2019.09.003
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