Søgeresultater - Kang, DongYang

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  1. 1
    A follow‐up study of a Chinese family with Waardenburg syndrome type II caused by a truncating mutation of MITF gene

    A follow‐up study of a Chinese family with Waardenburg syndrome type II caused by a truncating mutation of MITF gene af Yang, Shuzhi, Wang, Cuicui, Zhou, Chengyong, Kang, DongYang, Zhang, Xin, Yuan, Huijun

    Udgivet 2020
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  2. 2
    Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families

    Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families af Su, Yu, Gao, Xue, Huang, Sha-Sha, Mao, Jing-Ning, Huang, Bang-Qing, Zhao, Jian-Dong, Kang, Dong-Yang, Zhang, Xin, Dai, Pu

    Udgivet 2018
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  3. 3
    Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation

    Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation af Guo, Chang, Huang, Sha-Sha, Yuan, Yong-Yi, Zhou, Ying, Wang, Ning, Kang, Dong-Yang, Yang, Su-Yan, Zhang, Xin, Gao, Xue, Dai, Pu

    Udgivet 2020
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  4. 4
    Targeted Gene Capture and Massively Parallel Sequencing Identify TMC1 as the Causative Gene in a Six-generation Chinese Family with Autosomal Dominant Hearing Loss

    Targeted Gene Capture and Massively Parallel Sequencing Identify TMC1 as the Causative Gene in a Six-generation Chinese Family with Autosomal Dominant Hearing Loss af Gao, Xue, Huang, Sha-Sha, Yuan, Yong-Yi, Wang, Guo-Jian, Xu, Jin-Cao, Ji, Yu-Bin, Han, Ming-Yu, Yu, Fei, Kang, Dong-Yang, Lin, Xi, Dai, Pu

    Udgivet 2015
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  5. 5
    Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss

    Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss af Cui, Tian-Yi, Gao, Xue, Huang, Sha-Sha, Sun, Yan-Yan, Zhang, Si-Qi, Jiang, Xin-Xia, Yang, Yan-Zhong, Kang, Dong-Yang, Zhu, Qing-Wen, Yuan, Yong-Yi

    Udgivet 2020
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  6. 6
    Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss

    Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss af Wang, Wei-Qian, Gao, Xue, Huang, Sha-Sha, Kang, Dong-Yang, Xu, Jin-Cao, Yang, Kun, Han, Ming-Yu, Zhang, Xin, Yang, Su-Yan, Yuan, Yong-Yi, Dai, Pu

    Udgivet 2022
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  7. 7
    Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

    Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population af Gao, Xue, Huang, Sha-Sha, Yuan, Yong-Yi, Xu, Jin-Cao, Gu, Ping, Bai, Dan, Kang, Dong-Yang, Han, Ming-Yu, Wang, Guo-Jian, Zhang, Mei-Guang, Li, Jia, Dai, Pu

    Udgivet 2017
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  8. 8
    Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing

    Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing af Gao, Xue, Zhu, Qing-yan, Song, Yue-Shuai, Wang, Guo-Jian, Yuan, Yong-Yi, Xin, Feng, Huang, Sha-Sha, Kang, Dong-Yang, Han, Ming-Yu, Guan, Li-ping, Zhang, Jian-guo, Dai, Pu

    Udgivet 2013
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  9. 9
    A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family

    A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family af Gao, Xue, Xu, Jin-Cao, Wang, Wei-Qian, Yuan, Yong-Yi, Bai, Dan, Huang, Sha-Sha, Wang, Guo-Jian, Su, Yu, Li, Jia, Kang, Dong-Yang, Zhang, Mei-Guang, Lin, Xi, Dai, Pu

    Udgivet 2018
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  10. 10
    Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family

    Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family af Gao, Xue, Su, Yu, Chen, Yu-Lan, Han, Ming-Yu, Yuan, Yong-Yi, Xu, Jin-Cao, Xin, Feng, Zhang, Mei-Guang, Huang, Sha-Sha, Wang, Guo-Jian, Kang, Dong-Yang, Guan, Li-Ping, Zhang, Jian-Guo, Dai, Pu

    Udgivet 2015
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  11. 11
    A Novel Mutation in the TECTA Gene in a Chinese Family with Autosomal Dominant Nonsyndromic Hearing Loss

    A Novel Mutation in the TECTA Gene in a Chinese Family with Autosomal Dominant Nonsyndromic Hearing Loss af Su, Yu, Tang, Wen-Xue, Gao, Xue, Yu, Fei, Dai, Zhi-Yao, Zhao, Jian-Dong, Lu, Yu, Ji, Fei, Huang, Sha-Sha, Yuan, Yong-Yi, Han, Ming-Yu, Song, Yue-Shuai, Zhu, Yu-Hua, Kang, Dong-Yang, HAN, Dong-Yi, Dai, Pu

    Udgivet 2014
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  12. 12
    Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss

    Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss af Gao, Xue, Yuan, Yong-Yi, Lin, Qiong-Fen, Xu, Jin-Cao, Wang, Wei-Qian, Qiao, Yue-Hua, Kang, Dong-Yang, Bai, Dan, Xin, Feng, Huang, Sha-Sha, Qiu, Shi-Wei, Guan, Li-Ping, Su, Yu, Wang, Guo-Jian, Han, Ming-Yu, Jiang, Yi, Liu, Han-Kui, Dai, Pu

    Udgivet 2018
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  13. 13
    Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China

    Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China af Dai, Pu, Huang, Li-Hui, Wang, Guo-Jian, Gao, Xue, Qu, Chun-Yan, Chen, Xiao-Wei, Ma, Fu-Rong, Zhang, Jie, Xing, Wan-Li, Xi, Shu-Yan, Ma, Bin-Rong, Pan, Ying, Cheng, Xiao-Hua, Duan, Hong, Yuan, Yong-Yi, Zhao, Li-Ping, Chang, Liang, Gao, Ru-Zhen, Liu, Hai-Hong, Zhang, Wei, Huang, Sha-Sha, Kang, Dong-Yang, Liang, Wei, Zhang, Ke, Jiang, Hong, Guo, Yong-Li, Zhou, Yi, Zhang, Wan-Xia, Lyu, Fan, Jin, Ying-Nan, Zhou, Zhen, Lu, Hong-Li, Zhang, Xin, Liu, Ping, Ke, Jia, Hao, Jin-Sheng, Huang, Hai-Meng, Jiang, Di, Ni, Xin, Long, Mo, Zhang, Luo, Qiao, Jie, Morton, Cynthia Casson, Liu, Xue-Zhong, Cheng, Jing, Han, De-Min

    Udgivet 2019
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