Progress in Diagnosis and Treatment of Children having Fabry Disease by LI Xiaoxue, LIU Xiaorong

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A Case of Renal Coloboma Syndrome Caused by Spontaneous Mutation of PAX2 by LING Chen, CHEN Zhi, LIU Xiaorong

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Clinical, Pathological and Genetic Analysis of Alport Syndrome in Children by NI Jie, CHEN Zhi, LING Chen, LIU Xiaorong

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A multiplex recombinase polymerase amplification assay combined with CRISPR/Cas12a for the detection of respiratory syncytial virus and respiratory adenovirus by Gao Hongdan, Du Yao, Chai Qiang, Huang Meng, Liu Xiaorong, Xing Zhihao, Ma Dongli

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Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity by Souma, Tomokazu, Tompson, Stuart W., Thomson, Benjamin R., Siggs, Owen M., Kizhatil, Krishnakumar, Yamaguchi, Shinji, Feng, Liang, Limviphuvadh, Vachiranee, Whisenhunt, Kristina N., Maurer-Stroh, Sebastian, Yanovitch, Tammy L., Kalaydjieva, Luba, Azmanov, Dimitar N., Finzi, Simone, Mauri, Lucia, Javadiyan, Shahrbanou, Souzeau, Emmanuelle, Zhou, Tiger, Hewitt, Alex W., Kloss, Bethany, Burdon, Kathryn P., Mackey, David A., Allen, Keri F., Ruddle, Jonathan B., Lim, Sing-Hui, Rozen, Steve, Tran-Viet, Khanh-Nhat, Liu, Xiaorong, John, Simon, Wiggs, Janey L., Pasutto, Francesca, Craig, Jamie E., Jin, Jing, Quaggin, Susan E., Young, Terri L.

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