A Model of Waardenburg Syndrome Using Patient-Derived iPSCs With a SOX10 Mutation Displays Compromised Maturation and Function of the Neural Crest That Involves Inner Ear Developme... by Jie Wen, Jie Wen, Jie Wen, Jian Song, Jian Song, Jian Song, Yijiang Bai, Yijiang Bai, Yijiang Bai, Yalan Liu, Yalan Liu, Yalan Liu, Xinzhang Cai, Xinzhang Cai, Xinzhang Cai, Lingyun Mei, Lingyun Mei, Lingyun Mei, Lu Ma, Chufeng He, Chufeng He, Chufeng He, Yong Feng, Yong Feng

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Short-term effects of intravenous batroxobin in treatment of sudden sensorineural hearing loss: a propensity score-matched study by Mengzhu Jiang, Mengzhu Jiang, Huping Huang, Huping Huang, Lingyun Mei, Lingyun Mei, Lingyun Mei, Chufeng He, Chufeng He, Chufeng He, Xinzhang Cai, Xinzhang Cai, Xinzhang Cai, Lu Jiang, Lu Jiang, Lu Jiang, Hong Wu, Hong Wu, Hong Wu, Xin Wang, Xin Wang, Xuewen Wu, Xuewen Wu, Xuewen Wu

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A comprehensive genotype–phenotype evaluation of eight Chinese probands with Waardenburg syndrome by Sijun Li, Mengyao Qin, Shuang Mao, Lingyun Mei, Xinzhang Cai, Yong Feng, Chufeng He, Jian Song

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New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing by Wu Li, Lingyun Mei, Hongsheng Chen, Xinzhang Cai, Yalan Liu, Meichao Men, Xue Zhong Liu, Denise Yan, Jie Ling, Yong Feng

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A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing. by Yalan Liu, Lili Wang, Yong Feng, Chufeng He, Deyuan Liu, Xinzhang Cai, Lu Jiang, Hongsheng Chen, Chang Liu, Hong Wu, Lingyun Mei

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A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family. by Zhijie Niu, Yong Feng, Lingyun Mei, Jie Sun, Xueping Wang, Juncheng Wang, Zhengmao Hu, Yunpeng Dong, Hongsheng Chen, Chufeng He, Yalan Liu, Xinzhang Cai, Xuezhong Liu, Lu Jiang

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Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families by Shushan Sang, Shushan Sang, Jie Ling, Jie Ling, Jie Ling, Xuezhong Liu, Xuezhong Liu, Xuezhong Liu, Lingyun Mei, Lingyun Mei, Xinzhang Cai, Xinzhang Cai, Taoxi Li, Taoxi Li, Taoxi Li, Wu Li, Wu Li, Meng Li, Meng Li, Jie Wen, Jie Wen, Xianlin Liu, Xianlin Liu, Jing Liu, Jing Liu, Yalan Liu, Yalan Liu, Hongsheng Chen, Hongsheng Chen, Chufeng He, Chufeng He, Yong Feng, Yong Feng, Yong Feng, Yong Feng

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Modeling of auditory neuropathy spectrum disorders associated with the TEME43 variant reveals impaired gap junction function of iPSC-derived glia-like support cells by Xiaoming Kang, Xiaoming Kang, Lu Ma, Lu Ma, Lu Ma, Jie Wen, Jie Wen, Wei Gong, Wei Gong, Xianlin Liu, Xianlin Liu, Yihan Hu, Yihan Hu, Zhili Feng, Zhili Feng, Qiancheng Jing, Qiancheng Jing, Yuexiang Cai, Yuexiang Cai, Sijun Li, Xinzhang Cai, Kai Yuan, Yong Feng, Yong Feng, Yong Feng, Yong Feng, Yong Feng

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