Genetic etiology and pregnancy outcomes of fetal hyperechoic kidneys: a retrospective analysis by Meiying Cai, Na Lin, Ziheng Xiao, Ziheng Xiao, Hailong Huang, Lin Zheng, Liangpu Xu

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Ultrasound Phenotype, Genetic Analysis, and Pregnancy Outcomes of Fetuses With 1p36 Deletion Syndrome by Meiying Cai, Na Lin, Xuemei Chen, Hailong Huang, Nan Guo, Jiansong Lin, Liangpu Xu

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Comparative performance and health economic analysis of prenatal screening for down syndrome in Fujian province, China by Lin Zheng, Nuolan Yin, Meiying Wang, Hailong Huang, Shuyu Zhang, Linjuan Su, Liangpu Xu

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Etiology and outcomes of fetal renal abnormalities in Southern China: a single-tertiary-center study by Meiying Cai, Yashi Gao, Huili Xue, Xianguo Fu, Hua Cao, Liangpu Xu, Na Lin, Hailong Huang

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Hematological analysis of alpha-thalassemia: A single-center, retrospective clinical study by Lin Zheng, Nuolan Yin, Meiying Wang, Hailong Huang, Na Lin, Shuyu Zhang, Linjuan Su, Liangpu Xu

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Hematological analysis of alpha-thalassemia: A single-center, retrospective clinical study. by Lin Zheng, Nuolan Yin, Meiying Wang, Hailong Huang, Na Lin, Shuyu Zhang, Linjuan Su, Liangpu Xu

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Fujian Province β-Thalassemia: A Molecular and Hematological Study in Southeastern China by Junhao Zheng, Meihuan Chen, Siwen Zhang, Aixiang Lv, Min Zhang, Lingji Chen, Na Lin, Liangpu Xu, Hailong Huang

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Upregulation of miR-17-3p is associated with HbF in patients with β-thalassemia and induces γ-globin expression by targeting BCL11A by Siwen Zhang, Meihuan Chen, Wantong Zhao, Junhao Zheng, Yanhong Zhang, Aixiang Lv, Jingmin Li, Hua Cao, Liangpu Xu, Hailong Huang

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Regional patterns of genetic variants in expanded carrier screening: a next-generation sequencing pilot study in Fujian Province, China by Danhua Guo, Danhua Guo, Nani Zhou, Qianqian He, Qianqian He, Na Lin, Na Lin, Shuqiong He, Shuqiong He, Deqin He, Deqin He, Yifang Dai, Yifang Dai, Ying Li, Ying Li, Xuemei Chen, Xuemei Chen, Hailong Huang, Hailong Huang, Jia Jia, Hua Cao, Liangpu Xu, Liangpu Xu

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Prenatally and postnatally sequential genetic etiology detection in corpus callosum abnormalities by Huili Xue, Aili Yu, Lin Zheng, Xianglan Ye, Lin Zhang, Qun Guo, Lingji Chen, Qingmei Shen, Na lin, Hailong Huang, Liangpu Xu

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Incidental finding of a DMD exons 48–55 deletion during prenatal diagnosis by Min Zhang, Zhaodong Lin, Meihuan Chen, Danhua Guo, Qiaomei Yang, Qianqian He, Bin Mao, Bin Liang, Lingji Chen, Meiying Cai, Hailong Huang, Liangpu Xu

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Congenital muscular dystrophies and myopathies: the leading cause of genetic muscular disorders in eleven Chinese families by Bin Mao, Xiaoling Cai, Na Lin, Yulin Jiang, Na Hao, Yifang Dai, Danhua Guo, Deqin He, Huili Xue, Lingji Chen, Qianqian He, Min Zhang, Meihuan Chen, Hailong Huang, Liangpu Xu

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