Search Results - Fengxia Yao

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    Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome by Chao Ling, Ruifang Sui, Fengxia Yao, Zhihong Wu, Xue Zhang, Shuyang Zhang

    Published 2019
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    Prenatal Diagnosis of Dystrophinopathy and Cytogenetic Analysis in 303 Chinese Families by Mengmeng Li, Na Hao, Fengxia Yao, Weimin Zhang, Jing Zhou, Li Tan, Zhengqing Qiu, Juntao Liu, Yang Pan

    Published 2021
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