खोज परिणाम - Xiong Wang

  • प्रदर्शित 1 - 13 परिणाम 13
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  1. 1

    Exacerbation of ichthyosis vulgaris phenotype by co-inheritance of STS and FLG mutations in a Chinese family with ichthyosis: a case report द्वारा Xiong Wang, Lu Tan, Na Shen, Yanjun Lu, Ying Zhang

    प्रकाशित 2018
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  2. 2

    Hemophagocytic lymphohistiocytosis and congenital factor VII deficiency: a case report द्वारा Xiong Wang, Ning Tang, Wei Chang, Yanjun Lu, Dengju Li

    प्रकाशित 2018
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  3. 3

    Alpha and beta-Thalassemia mutations in Hubei area of China द्वारा Yaowu Zhu, Na Shen, Xiong Wang, Juan Xiao, Yanjun Lu

    प्रकाशित 2020
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  4. 4

    A novel TSC2 c.4511 T > C missense variant associated with tuberous sclerosis complex द्वारा Shunzhi He, Na Lv, Hongchu Bao, Xiong Wang, Jing Li

    प्रकाशित 2020
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  5. 5

    Novel NOG (p.P42S) mutation causes proximal symphalangism in a four-generation Chinese family द्वारा Yanwei Sha, Ding Ma, Ning Zhang, Xiaoli Wei, Wensheng Liu, Xiong Wang

    प्रकाशित 2019
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    A novel mutation in TRIOBP gene leading to congenital deafness in a Chinese family द्वारा Bingxin Zhou, Lili Yu, Yan Wang, Wenjing Shang, Yi Xie, Xiong Wang, Fengchan Han

    प्रकाशित 2020
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  8. 8

    Deficiency of mindin reduces renal injury after ischemia reperfusion द्वारा Tao Bai, Xiong Wang, Cong Qin, Kang Yang, Zhiguo Duan, Zhixiu Cao, Jiaqian Liang, Lei Wang, Jingdong Yuan, Pengcheng Luo

    प्रकाशित 2022
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  9. 9

    Levels of trace metals and their impact on oocyte: A review द्वारा Ping-Ping Zhang, Gui-Chun Ding, Chen-Yue Tao, Lei Zhang, Yi-Xiong Wang, Qiu-Yue Yuan, Sheng-Min Zhang, Li-Ping Wang

    प्रकाशित 2024
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    A novel nonsense mutation in ARMC5 causes primary bilateral macronodular adrenocortical hyperplasia द्वारा Wen-Tao He, Xiong Wang, Wen Song, Xiao-Dong Song, Yan-Jun Lu, Yan-Kai Lv, Ting He, Xue-Feng Yu, Shu-Hong Hu

    प्रकाशित 2021
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