Systematic estimation of cystic fibrosis prevalence in Chinese and genetic spectrum comparison to Caucasians by Qi Ni, Xiang Chen, Ping Zhang, Lin Yang, Yulan Lu, Feifan Xiao, Bingbing Wu, Huijun Wang, Wenhao Zhou, Xinran Dong

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High-Frequency Exon Deletion of DNA Cross-Link Repair 1C Accounting for Severe Combined Immunodeficiency May Be Missed by Whole-Exome Sequencing by Feifan Xiao, Yulan Lu, Bingbing Wu, Bo Liu, Gang Li, Ping Zhang, Qinhua Zhou, Jinqiao Sun, Huijun Wang, Wenhao Zhou, Wenhao Zhou

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Overdosage of HNF1B Gene Associated With Annular Pancreas Detected in Neonate Patients With 17q12 Duplication by Feifan Xiao, Feifan Xiao, Xiuyun Liu, Xiuyun Liu, Yulan Lu, Bingbing Wu, Renchao Liu, Bo Liu, Kai Yan, Huiyao Chen, Huiyao Chen, Guoqiang Cheng, Laishuan Wang, Qi Ni, Qi Ni, Gang Li, Ping Zhang, Xiaomin Peng, Yun Cao, Chun Shen, Huijun Wang, Wenhao Zhou, Wenhao Zhou, Wenhao Zhou

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Combining Metagenomic Sequencing With Whole Exome Sequencing to Optimize Clinical Strategies in Neonates With a Suspected Central Nervous System Infection by Mengmeng Ge, Mingyu Gan, Kai Yan, Feifan Xiao, Lin Yang, Bingbing Wu, Mili Xiao, Yin Ba, Rong Zhang, Jin Wang, Guoqiang Cheng, Laishuan Wang, Yun Cao, Wenhao Zhou, Wenhao Zhou, Liyuan Hu

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Neonatal Metabolic Acidosis in the Neonatal Intensive Care Unit: What Are the Genetic Causes? by Haiyan Ma, Zezhong Tang, Feifan Xiao, Long Li, Yangfang Li, Wenyan Tang, Liping Chen, Wenqing Kang, Yulan Lu, Xinran Dong, Guoqiang Cheng, Laishuan Wang, Wei Lu, Lin Yang, Qi Ni, Xiaomin Peng, Yao Wang, Yun Cao, Bingbing Wu, Wenhao Zhou, Wenhao Zhou, Deyi Zhuang, Guang Lin, Huijun Wang

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