Risultati della ricerca - Pengzhen Jin

Case report: A compound heterozygous mutations in ASNS broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis di 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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Molecular diagnostic yield of exome sequencing in a Chinese cohort of 512 fetuses with anomalies di Pengzhen Jin, Jiawei Hong, Yuqing Xu, Yeqing Qian, Shuning Han, Minyue Dong

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Identification of four TTN variants in three families with fetal akinesia deformation sequence di 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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