The clinical application and laboratory management of molecular genetic diagnosis in children's hospital by Wenjie Bao, Qihua Fu, Xiaoqing Zhang, Xi Mo, Tingting Yu

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Development of two different pharmacogenomics detection methods for second-generation antipsychotic drugs quetiapine and aripiprazole by Lichen Zhang, Xingyu Zhang, Xiaoqing Zhang, Guoling You, Qihua Fu

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Blood arsenic exposure levels of preschool children and dietary factors analysis by Junxia LIU, Zhenyan GAO, Ju WANG, Chenyin DONG, Chonghuai YAN, Qihua FU

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Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies by Yibo Lu, Yiyang Zhou, Jing Guo, Ming Qi, Yuwan Lin, Xingyu Zhang, Ying Xiang, Qihua Fu, Bo Wang

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Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease by Yibo Lu, Qing Fang, Ming Qi, Xiaoliang Li, Xingyu Zhang, Yuwan Lin, Ying Xiang, Qihua Fu, Bo Wang

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MET mutation causes muscular dysplasia and arthrogryposis by Hang Zhou, Chengjie Lian, Tingting Wang, Xiaoming Yang, Caixia Xu, Deying Su, Shuhui Zheng, Xiangyu Huang, Zhiheng Liao, Taifeng Zhou, Xianjian Qiu, Yuyu Chen, Bo Gao, Yongyong Li, Xudong Wang, Guoling You, Qihua Fu, Christina Gurnett, Dongsheng Huang, Peiqiang Su

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Bi-allelic variants in CEP295 cause Seckel-like syndrome presenting with primary microcephaly, developmental delay, intellectual disability, short stature, craniofacial and digital... by Niu Li, Yufei Xu, Hongzhu Chen, Jingqi Lin, Lama AlAbdi, Mir Reza Bekheirnia, Guoqiang Li, Yoel Gofin, Nasim Bekheirnia, Eissa Faqeih, Lina Chen, Guoying Chang, Jie Tang, Ruen Yao, Tingting Yu, Xiumin Wang, Wei Fu, Qihua Fu, Yiping Shen, Fowzan S. Alkuraya, Keren Machol, Jian Wang

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