Prenatal diagnosis and genetic counseling of a 10p11.23q11.21 duplication associated with normal phenotype by Jieping Song, Wei Jiang, Chengcheng Zhang, Bo Wang

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A rare case of uniparental isodisomy of chromosome 19 with no phenotypic abnormalities by Jieping Song, Ling Zhu, Ting Zhou, Bo Wang

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A rare case of complete uniparental isodisomy of chromosome 2 with no phenotypic abnormalities by Jieping Song, Ling Zhu, Chengcheng Zhang, Ying Wu, Bo Wang

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Clinical and genetic study of three families with 15q11q13 duplications by Jieping Song, Xu Liu, Chengcheng Zhang, Fei Xu, Bo Wang

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The value of 68Ga-PSMA PET/CT in the diagnosis of intracapsular prostate cancer with a poor prognosis by Yajing Wang, Jieping Song, Lulu Yang, Wencheng Li, Wei Wang, Aiqing Ji, Liwei Wang, Feng Wang

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Prenatal diagnosis and outcomes in 320 fetuses with nasal bone anomalies by Hui Li, Yanyi Yao, Chengcheng Zhang, Yayun Qin, Ling Zeng, Jieping Song, Li Lu, Wei Wang, Lijun Liu

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Perinatal outcomes of prenatal cases testing positive for trisomy 9 by noninvasive prenatal testing by Hui Li, Li Lu, Yanyi Yao, Tangxinzi Gao, Yufei Jiang, Chengcheng Zhang, Nian Liu, Jieping Song, Wei Wang, Lijun Liu

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Prenatal whole-exome sequencing for fetal structural anomalies: a retrospective analysis of 145 Chinese cases by Yayun Qin, Yanyi Yao, Nian Liu, Bo Wang, Lijun Liu, Hui Li, Tangxinzi Gao, Runhong Xu, Xiaoyan Wang, Fanglian Zhang, Jieping Song

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A feasibility study of noninvasive prenatal diagnosis in facioscapulohumeral muscular dystrophy type 1 in a Chinese family by Yayun Qin, Hui Xu, Jingmin Yang, Jingmin Yang, Jingmin Yang, Yiming Wu, Hui Li, Bo Wang, Lijun Liu, Ding Ren, Runhong Xu, Manman Li, Chengcheng Zhang, Jieping Song

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Clinical efficiency of simultaneous CNV-seq and whole-exome sequencing for testing fetal structural anomalies by Xinlin Chen, Yulin Jiang, Ruiguo Chen, Qingwei Qi, Xiujuan Zhang, Sheng Zhao, Chaoshi Liu, Weiyun Wang, Yuezhen Li, Guoqiang Sun, Jieping Song, Hui Huang, Chen Cheng, Jianguang Zhang, Longxian Cheng, Juntao Liu

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Genomic architecture of fetal central nervous system anomalies using whole-genome sequencing by Ying Yang, Sheng Zhao, Guoqiang Sun, Fang Chen, Tongda Zhang, Jieping Song, Wenzhong Yang, Lin Wang, Nianji Zhan, Xiaohong Yang, Xia Zhu, Bin Rao, Zhenzhen Yin, Jing Zhou, Haisheng Yan, Yushan Huang, Jingyu Ye, Hui Huang, Chen Cheng, Shida Zhu, Jian Guo, Xun Xu, Xinlin Chen

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Genetic deconvolution of fetal and maternal cell-free DNA in maternal plasma enables next-generation non-invasive prenatal screening by Chenming Xu, Jianli Li, Songchang Chen, Xiaoqiang Cai, Ruilin Jing, Xiaomei Qin, Dong Pan, Xin Zhao, Dongyang Ma, Xiufeng Xu, Xiaojun Liu, Can Wang, Bingxin Yang, Lanlan Zhang, Shuyuan Li, Yiyao Chen, Nina Pan, Ping Tang, Jieping Song, Nian Liu, Chen Zhang, Zhiwei Zhang, Xiang Qiu, Weiliang Lu, Chunmei Ying, Xiaotian Li, Congjian Xu, Yanlin Wang, Yanting Wu, He-Feng Huang, Jinglan Zhang

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