Hasil Pencarian - Baicheng Xu

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  1. 1
    Research Advances on Deafness Genes Associated with Mitochondrial tRNA-37 Modifications

    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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  2. 2
    Holographic response from higher derivatives with homogeneous disorder

    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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  3. 3
    Study on the correlation between ambient environment-meteorological factors and the number of visits of acute otitis media, Lanzhou, China

    Study on the correlation between ambient environment-meteorological factors and the number of visits of acute otitis media, Lanzhou, China oleh Haiyue Tian, Baicheng Xu, Xinlan Wang, Jinyan Wang, Cuiping Zhong

    Diterbitkan 2020-09-01
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  4. 4
    Screening of SLC26A4 Gene Hotspots in 2673 Patients Associated with Sensorineural Hearing Loss in Northwestern China

    Screening of SLC26A4 Gene Hotspots in 2673 Patients Associated with Sensorineural Hearing Loss in Northwestern China oleh Yanli Wang, Yong Li, Baicheng Xu, Yiming Zhu, Xingjian Chen, Yufen Guo

    Diterbitkan 2022-03-01
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  5. 5
    Verification of an iPSC line (LZUi002-A) from a patient with a novel mutation in the TBL1X gene

    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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  6. 6
    A rare transcript homozygous variants in CLRN1(USH3A) causes Usher syndrome type 3 in a Chinese family

    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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  7. 7
    A novel intronic variant causing aberrant splicing identified in two deaf Chinese siblings with enlarged vestibular aqueducts

    A novel intronic variant causing aberrant splicing identified in two deaf Chinese siblings with enlarged vestibular aqueducts oleh Suyang Wang, Yi‐Ming Zhu, ChenYang Xu, Wenjuan Ding, Hui Jia, Panpan Bian, Baicheng Xu, Yufen Guo, Xiaowen Liu

    Diterbitkan 2024-02-01
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  8. 8
    Analysis of GJB2 Gene Mutations in 1330 Deafness Cases of Major Ethnic Groups in Northwest China

    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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  9. 9
    Targeted Next Generation Sequencing Revealed a Novel Homozygous Loss-of-Function Mutation in ILDR1 Gene Causes Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss in a Chinese Family

    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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