Hasil Pencarian - Baicheng Xu
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Research Advances on Deafness Genes Associated with Mitochondrial tRNA-37 Modifications oleh Panpan Bian, Jing Chai, Baicheng Xu
Diterbitkan 2023-09-01
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Holographic response from higher derivatives with homogeneous disorder oleh Guoyang Fu, Jian-Pin Wu, Baicheng Xu, Jiaqiu Liu
Diterbitkan 2017-06-01
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Verification of an iPSC line (LZUi002-A) from a patient with a novel mutation in the TBL1X gene oleh Yanli Wang, Zengping Liu, Chi Chen, Yong Li, Minxin Guan, Baicheng Xu, Yufen Guo
Diterbitkan 2022-05-01
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A rare transcript homozygous variants in CLRN1(USH3A) causes Usher syndrome type 3 in a Chinese family oleh Suyang Wang, Chen Yang Xu, Yiming Zhu, Wenjuan Ding, Jieyu Hu, Baicheng Xu, Yufen Guo, Xiaowen Liu
Diterbitkan 2024-09-01
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Analysis of GJB2 Gene Mutations in 1330 Deafness Cases of Major Ethnic Groups in Northwest China oleh Panpan Bian Master, Baicheng Xu Doctor, Xiaoyun Zhao Master, YiMing Zhu Doctor, Chi Chen Master, XingJian Chen Master, Xiaowen Liu Doctor, Yanli Wang Master, Yufen Guo Doctor
Diterbitkan 2022-10-01
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Targeted Next Generation Sequencing Revealed a Novel Homozygous Loss-of-Function Mutation in ILDR1 Gene Causes Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss in a Chin... oleh Jinxia An, Jie Yang, Yan Wang, Yanxia Wang, Baicheng Xu, Guangmei Xie, Sanming Chai, Xiaoling Liu, Sijuan Xu, Xiaoxiao Wen, Qing He, Huijun Liu, Chen Li, Subrata Kumar Dey, Yali Ni, Santasree Banerjee
Diterbitkan 2019-02-01
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