Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of LAMA2 gene by Yuqing Xu, Yuqing Xu, Linyan Zhu, Yeqing Qian, Yeqing Qian, Minyue Dong, Minyue Dong

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Novel homozygous silent mutation of ITGB3 gene caused Glanzmann thrombasthenia by Zhengrong Wang, Zhengrong Wang, Yuqing Xu, Yuqing Xu, Yixi Sun, Yixi Sun, Shuang Wang, Shuang Wang, Minyue Dong, Minyue Dong

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Case report: A compound heterozygous mutations in ASNS broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis by Linyan Zhu, Linyan Zhu, Yixi Sun, Yixi Sun, Yuqing Xu, Yuqing Xu, Pengzhen Jin, Pengzhen Jin, Huiqing Ding, Minyue Dong, Minyue Dong

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Down-Regulation of PLAC1 in the Placenta of Gestational Diabetes Mellitus Patients and its Clinical Significance by Mengkai Du, Yanmin Chen, Minyue Dong, Zhaoxia Liang, Danqing Chen

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Molecular diagnostic yield of exome sequencing in a Chinese cohort of 512 fetuses with anomalies by Pengzhen Jin, Jiawei Hong, Yuqing Xu, Yeqing Qian, Shuning Han, Minyue Dong

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Alteration in methylation level at differential methylated regions of MEST and DLK1 in fetus of preeclampsia by Xiaoqing Wang, Liuxia Wan, Xiaoling Weng, Jiamin Xie, Aiping Zhang, Yun Liu, Minyue Dong

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Efficiency of non-invasive prenatal screening in pregnant women at advanced maternal age by Hui Zhu, Xiaoxiao Jin, Yuqing Xu, Weihua Zhang, Xiaodan Liu, Jinglei Jin, Yeqing Qian, Minyue Dong

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Identification of four TTN variants in three families with fetal akinesia deformation sequence by Lihong Fan, Haibo Li, Ying Xu, Yingzhi Huang, Yeqing Qian, Pengzhen Jin, Xueping Shen, Zhi Li, Mingsong Liu, Yufei Liang, Guosong Shen, Minyue Dong

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