Study on coherent coupling of multi-core PCFs by Yue-E. Chen, Qiu-Feng Shao

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Language Learning Enhanced by Massive Multiple Online Role-Playing Games (MMORPGs) and the Underlying Behavioral and Neural Mechanisms by Yongjun Zhang, Yongjun Zhang, Hongwen Song, Xiaoming Liu, Xiaoming Liu, Dinghong Tang, Yue-e Chen, Yue-e Chen, Xiaochu Zhang, Xiaochu Zhang, Xiaochu Zhang, Xiaochu Zhang, Xiaochu Zhang

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Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center ret... by Jianlong Zhuang, Na Zhang, Yu’e Chen, Yuying Jiang, Xinying Chen, Wenli Chen, Chunnuan Chen

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Deficient Biological Motion Perception in Schizophrenia: Results from a Motion Noise Paradigm by Jejoong eKim, Dan eNorton, Ryan eMcBain, Dost eOngur, Yue eChen

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Tuning photonic crystal fabrication by nanosphere lithography and surface treatment of AlGaN-based ultraviolet light-emitting diodes by Kuan W.A. Chee, Wei Guo, John R. Wang, Yong Wang, Yue-e Chen, Jichun Ye

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Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis‐van Creveld syndrome by Jianlong Zhuang, Shufen Liu, Junyu Wang, Yu'e Chen, Hegan Zhang, Yuying Jiang, Gaoxiong Wang, Chunnuan Chen

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Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication by Jianlong Zhuang, Chunnuan Chen, Yuanbai Wang, Shuhong Zeng, Yu’e Chen, Yuying Jiang, Yingjun Xie, Yingjun Xie, Gaoxiong Wang

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Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole‐exome sequencing: A rare case report and literature review by Jianlong Zhuang, Qi Luo, Meihua Xie, Yu’e Chen, Yuying Jiang, Shuhong Zeng, Yuanbai Wang, Yingjun Xie, Chunnuan Chen

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Catalytic Degradation of Triphenylmethane Dyes with an Iron Porphyrin Complex as a Cytochrome P450 Model by Xiaoyan Lu, Qiman Che, Xinkai Niu, Yilin Zhang, Yu’e Chen, Qing Han, Miaoqing Li, Shuang Wang, Jihong Lan

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The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray Analysis by Yu'e Chen, Yingjun Xie, Yingjun Xie, Yuying Jiang, Qi Luo, Lijing Shi, Shuhong Zeng, Jianlong Zhuang, Guorong Lyu

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Identification of a Rare Variant of c.1777G>A (p.G593S) in the COL1A1 Gene as the Etiology of Recurrent Osteogenesis Imperfecta by Whole-Exome Sequencing by Jianlong Zhuang, Chunnuan Chen, Yu'e Chen, Qi Luo, Yuanbai Wang, Yuying Jiang, Shuhong Zeng, Yingjun Xie, Yingjun Xie, Dongmei Chen

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Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing by Jianlong Zhuang, Chunnuan Chen, Yu’e Chen, Shuhong Zeng, Yuying Jiang, Yuanbai Wang, Xinying Chen, Yingjun Xie, Yingjun Xie, Gaoxiong Wang

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Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report by Jianlong Zhuang, Junyu Wang, Qi Luo, Shuhong Zeng, Yu’e Chen, Yuying Jiang, Xinying Chen, Yuanbai Wang, Yingjun Xie, Yingjun Xie, Gaoxiong Wang, Chunnuan Chen

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Etiology analysis and G6PD deficiency for term infants with jaundice in Yangjiang of western Guangdong by Yi-Kang Yang, Yi-Kang Yang, Chun-Fan Lin, Fen Lin, Zi-Kai Chen, Yu-Wei Liao, Yu-Wei Liao, Yu-Chan Huang, Yu-Chan Huang, Bei-Ru Xiao, Shan-Hua Huang, Yu-Mei Xu, Yue-E. Chen, Yan-Bin Cao, Yan-Bin Cao, Li-Ye Yang, Li-Ye Yang

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Covid-19 omicron variant infection in neonates of Guangdong province-a report of 52 cases by Yi-Kang Yang, Yi-Kang Yang, Fen Lin, Jian-Feng Lin, Chun-Fan Lin, Li-Li Liu, Yu-Bin Ma, Xian-Yao Wang, Yu-Wei Liao, Yu-Wei Liao, Yu-Chan Huang, Guang-Kuan Zeng, Bei-Ru Xiao, Shan-Hua Huang, Yu-Mei Xu, Yue-E Chen, Yan-Bin Cao, Li-Ye Yang, Li-Ye Yang

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