Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, China by Yan Wang, Min Zhang, Lingji Chen, Hailong Huang, Liangpu Xu

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Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center by Huili Xue, Aili Yu, Lingji Chen, Qun Guo, Lin Zhang, Na lin, Xuemei Chen, Liangpu Xu, Hailong Huang

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The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression. by Meihuan Chen, Xinrui Wang, Haiwei Wang, Min Zhang, Lingji Chen, Hong Chen, Yali Pan, Yanhong Zhang, Liangpu Xu, Hailong Huang

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Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing by Huili Xue, Aili Yu, Lin Zhang, Lingji Chen, Qun Guo, Min Lin, Na lin, Xuemei Chen, Liangpu Xu, Hailong Huang

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The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression by Meihuan Chen, Xinrui Wang, Haiwei Wang, Min Zhang, Lingji Chen, Hong Chen, Yali Pan, Yanhong Zhang, Liangpu Xu, Hailong Huang

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Prenatal diagnosis of fetal skeletal anomalies via whole-exome sequencing in a tertiary referral center by Huili Xue, Aili Yu, Wantong Zhao, Lingji Chen, Ruqi Fang, Wen Ling, Lin Zhang, Qun Guo, Na lin, Liangpu Xu, Hailong Huang

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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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