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American Journal of Human Genetics|December 22, 2009
Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2Xuezhong Liu, Dongyi Han, Jianzhong Li, et al.American Journal of Human Genetics|January 29, 2013
Genetic basis of Y-linked hearing impairmentQiuju Wang, Yali Xue, Yujun Zhang, et al.Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|July 25, 2024
Deep Learning-Enabled Vasculometry Depicts Phased Lesion Patterns in High Myopia ProgressionHai-Long He, Yi-Xin Liu, Hanruo Liu, et al.Nature Communications|May 5, 2018
CCDC102B confers risk of low vision and blindness in high myopiaYoshikatsu Hosoda, Munemitsu Yoshikawa, Masahiro Miyake, et al.Translational Psychiatry|February 19, 2021
Acute psychological impact on COVID-19 patients in Hubei: a multicenter observational studyMinghuan Wang, Caihong Hu, Qian Zhao, et al.Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|December 22, 2021
Validation of Soft Labels in Developing Deep Learning Algorithms for Detecting Lesions of Myopic Maculopathy From Optical Coherence Tomographic ImagesRan Du, Shiqi Xie, Yuxin Fang, et al.Journal of Affective Disorders|December 19, 2020
Prevalence of psychological disorders in the COVID-19 epidemic in China: A real world cross-sectional studyMinghuan Wang, Qian Zhao, Caihong Hu, et al.Journal of Translational Medicine|April 16, 2009
GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairmentPu Dai, Fei Yu, Bing Han, et al.Pageof 30