Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin–Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencing by Guanting Lu, Qiongling Peng, Lianying Wu, Jian Zhang, Liya Ma

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Restricted Kinematics in Children With Autism in the Execution of Complex Oscillatory Arm Movements by Zhong Zhao, Xiaobin Zhang, Haiming Tang, Xinyao Hu, Xingda Qu, Jianping Lu, Qiongling Peng

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Late-onset sepsis in very low birth weight preterm infants: 7 years' experience at a tertiary hospital in China by Liya Ma, Qiongling Peng, Wei Wang, Yi Yang, You Chen, Liling Wang, Hung-Chih Lin

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A de Novo ZMIZ1 Pathogenic Variant for Neurodevelopmental Disorder With Dysmorphic Facies and Distal Skeletal Anomalies by Guanting Lu, Liya Ma, Pei Xu, Binqiang Xian, Lianying Wu, Jianying Ding, Xiaoyan He, Huiyun Xia, Wuwu Ding, Zhirong Yang, Qiongling Peng

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A synonymous variant contributes to a rare Wiedemann-Rautenstrauch syndrome complicated with mild anemia via affecting pre-mRNA splicing by Qiongling Peng, Yan Zhang, Binqiang Xian, Lianying Wu, Lianying Wu, Jianying Ding, Wuwu Ding, Xin Zhang, Bilan Ding, Ding Li, Jin Wu, Xiaowu Hu, Guanting Lu, Guanting Lu

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Identification of a de novo mutation of the FOXG1 gene and comprehensive analysis for molecular factors in Chinese FOXG1-related encephalopathies by Guanting Lu, Guanting Lu, Yan Zhang, Huiyun Xia, Xiaoyan He, Xiaoyan He, Pei Xu, Pei Xu, Lianying Wu, Lianying Wu, Ding Li, Liya Ma, Jin Wu, Jin Wu, Qiongling Peng

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