Further delineation of phenotype and genotype of Kenny–Caffey syndrome type 2 (phenotype and genotype of KCS type 2) by Xuefei Chen, Chaochun Zou

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Microdeletion of 4p16.2 in Children: A Case Report and Literature Review by Yanjie Qian, Xiaoying Wang, Wei Tang, Chaochun Zou

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Metabolic profiling reveals altered amino acid and fatty acid metabolism in children with Williams Syndrome by Weijun Chen, Yang Yang, Yu Zhang, Changxuan Sun, Chai Ji, Jiyang Shen, Fangfang Li, Yingping Xiao, Yang Wen, Qian Liu, Chaochun Zou

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Using sno-lncRNAs as potential markers for Prader-Willi syndrome diagnosis by Jiu-Ru Sun, Liang-Zhong Yang, Yang-Li Dai, Huang Wu, Siqi Li, Yi-Feng Xu, Youkui Huang, Hao Wu, Zheng Shen, Chaochun Zou, Ling-Ling Chen

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Phosphorylation of human glioma-associated oncogene 1 on Ser937 regulates Sonic Hedgehog signaling in medulloblastoma by Ling-Hui Zeng, Chao Tang, Minli Yao, Qiangqiang He, Meiyu Qv, Qianlei Ren, Yana Xu, Tingyu Shen, Weizhong Gu, Chengyun Xu, Chaochun Zou, Xing Ji, Ximei Wu, Jirong Wang

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