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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Vydáno v:Am J Hum Genet
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Elsevier 2019
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Article
On-line přístup: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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