Hasil Pencarian - WeiYing Jiang

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  1. 1
    A novel Norrie disease pseudoglioma gene mutation, c.-1_2delAAT, responsible for Norrie disease in a Chinese family

    A novel Norrie disease pseudoglioma gene mutation, c.-1_2delAAT, responsible for Norrie disease in a Chinese family oleh Xin-Yu Zhang, Wei-Ying Jiang, Lu-Ming Chen, Su-Qin Chen

    Diterbitkan 2013-12-01
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  2. 2
    Identification of novel variations of oculocutaneous albinism type 2 with Prader–Willi syndrome/Angelman syndrome in two Chinese families

    Identification of novel variations of oculocutaneous albinism type 2 with Prader–Willi syndrome/Angelman syndrome in two Chinese families oleh XiaoFei Chen, XiaoFei Chen, ZiShui Fang, ZiShui Fang, Ting Pang, DongZhi Li, Jie Lei, Jie Lei, WeiYing Jiang, HongYi Li

    Diterbitkan 2023-03-01
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