Showing 1 - 9 results of 9 for search 'Dong-Yang Kang', query time: 0.04s Refine Results
  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 by Shuzhi Yang, Cuicui Wang, Chengyong Zhou, DongYang Kang, Xin Zhang, Huijun Yuan

    Published 2020-12-01
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  2. 2
    Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene

    Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene by Xue Gao, Shi–Wei Qiu, Wei-Qian Wang, Dong-Yang Kang, Ning Su, Pu Dai, Yong–Yi Yuan

    Published 2021-05-01
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  3. 3
    Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1B2

    Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1... by Xue Gao, Shi–Wei Qiu, Meng-Long Feng, Sha-Sha Huang, Dong-Yang Kang, Ming-Yu Han, Pu Dai, Yong–Yi Yuan

    Published 2020-10-01
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  4. 4
    Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families

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

    Published 2018-09-01
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  5. 5
    MPZL2—a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population

    MPZL2—a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population by Lang Zhang, Jin-Yuan Yang, Qiu-Quan Wang, Xue Gao, Guo-Jian Wang, Ming-Yu Han, Dong-Yang Kang, Dong-Yi Han, Sha-Sha Huang, Yong-Yi Yuan

    Published 2024-01-01
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  6. 6
    A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4

    A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4 by Kun Yang, Xi Wang, Wei‐Qian Wang, Ming‐Yu Han, Li‐Min Hu, Dong‐Yang Kang, Jin‐Yuan Yang, Min Liu, Xue Gao, Yong‐Yi Yuan, Jin‐Cao Xu

    Published 2023-03-01
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  7. 7
    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 by Wei-Qian Wang, Wei-Qian Wang, Xue Gao, Xue Gao, Sha-Sha Huang, Dong-Yang Kang, Jin-Cao Xu, Kun Yang, Ming-Yu Han, Xin Zhang, Su-Yan Yang, Yong-Yi Yuan, Pu Dai

    Published 2022-05-01
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  8. 8
    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. by Xue Gao, Yu Su, Yu-Lan Chen, Ming-Yu Han, Yong-Yi Yuan, Jin-Cao Xu, Feng Xin, Mei-Guang Zhang, Sha-Sha Huang, Guo-Jian Wang, Dong-Yang Kang, Li-Ping Guan, Jian-Guo Zhang, Pu Dai

    Published 2015-01-01
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  9. 9
    Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A

    Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site v... by Jin-Yuan Yang, Wei-Qian Wang, Ming-Yu Han, Sha-Sha Huang, Guo-Jian Wang, Yu Su, Jin-Cao Xu, Ying Fu, Dong-Yang Kang, Kun Yang, Xin Zhang, Xing Liu, Xue Gao, Yong-Yi Yuan, Pu Dai

    Published 2022-11-01
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