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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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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