Search Results - Xingkun Yang

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    Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome by Chao Li, Weiyao Luo, Tingting Xiao, Xingkun Yang, Miaoling Ou, Linghua Zhang, Xiang Huang, Xiaodan Zhu

    Published 2022
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    Case Report: A Novel Compound Heterozygous Mutation of the FRMD4A Gene Identified in a Chinese Family With Global Developmental Delay, Intellectual Disability, and Ataxia by Yuhua Pan, Xiaoling Guo, Xiaoqiang Zhou, Yue Liu, Jingli Lian, Tingting Yang, Xiang Huang, Fei He, Jian Zhang, Buling Wu, Fu Xiong, Fu Xiong, Fu Xiong, Xingkun Yang

    Published 2021
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