Hasil Pencarian - Yongchuan Chai

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  1. 1
    Treatment of congenital middle ear cholesteatoma in children using endoscopic and microscopic ear surgeries: a case series

    Treatment of congenital middle ear cholesteatoma in children using endoscopic and microscopic ear surgeries: a case series oleh Po Xue, Po Xue, Po Xue, Zhaoyan Wang, Zhaoyan Wang, Zhaoyan Wang, Yongchuan Chai, Yongchuan Chai, Yongchuan Chai, Mingjue Si, Lingxiang Hu, Lingxiang Hu, Lingxiang Hu

    Diterbitkan 2024-05-01
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  2. 2
    Detection and Functional Verification of Noncanonical Splice Site Mutations in Hereditary Deafness

    Detection and Functional Verification of Noncanonical Splice Site Mutations in Hereditary Deafness oleh Penghui Chen, Penghui Chen, Penghui Chen, Penghui Chen, Longhao Wang, Longhao Wang, Longhao Wang, Yongchuan Chai, Yongchuan Chai, Yongchuan Chai, Hao Wu, Hao Wu, Hao Wu, Tao Yang, Tao Yang, Tao Yang

    Diterbitkan 2021-12-01
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  3. 3
    Postnatal Development of Microglia-Like Cells in Mouse Cochlea

    Postnatal Development of Microglia-Like Cells in Mouse Cochlea oleh Penghui Chen, Yongchuan Chai, Haijin Liu, Gen Li, Longhao Wang, Tao Yang, Hao Wu

    Diterbitkan 2018-01-01
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  4. 4
    Characterization of spectrum, de novo rate and genotype-phenotype correlation of dominant GJB2 mutations in Chinese hans.

    Characterization of spectrum, de novo rate and genotype-phenotype correlation of dominant GJB2 mutations in Chinese hans. oleh Xiuhong Pang, Yongchuan Chai, Lianhua Sun, Dongye Chen, Ying Chen, Zhihua Zhang, Hao Wu, Tao Yang

    Diterbitkan 2014-01-01
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  5. 5
    A 1.6-Mb microdeletion in chromosome 17q22 leads to NOG-related symphalangism spectrum disorder without intellectual disability.

    A 1.6-Mb microdeletion in chromosome 17q22 leads to NOG-related symphalangism spectrum disorder without intellectual disability. oleh Xiuhong Pang, Huajie Luo, Yongchuan Chai, Xiaowen Wang, Lianhua Sun, Longxia He, Penghui Chen, Hao Wu, Tao Yang

    Diterbitkan 2015-01-01
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  6. 6
    Targeted next-generation sequencing in Uyghur families with non-syndromic sensorineural hearing loss.

    Targeted next-generation sequencing in Uyghur families with non-syndromic sensorineural hearing loss. oleh Ying Chen, Zhentao Wang, Zhaoyan Wang, Dongye Chen, Yongchuan Chai, Xiuhong Pang, Lianhua Sun, Xiaowen Wang, Tao Yang, Hao Wu

    Diterbitkan 2015-01-01
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  7. 7
    Identification and Characterization of a Cryptic Genomic Deletion-Insertion in EYA1 Associated with Branchio-Otic Syndrome

    Identification and Characterization of a Cryptic Genomic Deletion-Insertion in EYA1 Associated with Branchio-Otic Syndrome oleh Hao Zheng, Jun Xu, Yu Wang, Yun Lin, Qingqiang Hu, Xing Li, Jiusheng Chu, Changling Sun, Yongchuan Chai, Xiuhong Pang

    Diterbitkan 2021-01-01
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  8. 8
    The p.V37I exclusive genotype of GJB2: a genetic risk-indicator of postnatal permanent childhood hearing impairment.

    The p.V37I exclusive genotype of GJB2: a genetic risk-indicator of postnatal permanent childhood hearing impairment. oleh Lei Li, Jingrong Lu, Zheng Tao, Qi Huang, Yongchuan Chai, Xiaohua Li, Zhiwu Huang, Yun Li, Mingliang Xiang, Jun Yang, Guoyin Yao, Yu Wang, Tao Yang, Hao Wu

    Diterbitkan 2012-01-01
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  9. 9
    Impact of inner ear malformation and cochlear nerve deficiency on the development of auditory-language network in children with profound sensorineural hearing loss

    Impact of inner ear malformation and cochlear nerve deficiency on the development of auditory-language network in children with profound sensorineural hearing loss oleh Yaoxuan Wang, Mengda Jiang, Yuting Zhu, Lu Xue, Wenying Shu, Xiang Li, Hongsai Chen, Yun Li, Ying Chen, Yongchuan Chai, Yu Zhang, Yinghua Chu, Yang Song, Xiaofeng Tao, Zhaoyan Wang, Hao Wu

    Diterbitkan 2023-09-01
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  10. 10
    Association of GRM7 variants with different phenotype patterns of age-related hearing impairment in an elderly male Han Chinese population.

    Association of GRM7 variants with different phenotype patterns of age-related hearing impairment in an elderly male Han Chinese population. oleh Huajie Luo, Tao Yang, Xiaojie Jin, Xiuhong Pang, Jiping Li, Yongchuan Chai, Lei Li, Yi Zhang, Luping Zhang, Zhihua Zhang, Wenjing Wu, Qin Zhang, Xianting Hu, Jingwen Sun, Xuemei Jiang, Zhuping Fan, Zhiwu Huang, Hao Wu

    Diterbitkan 2013-01-01
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