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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 3, 2021
[Analysis of PHEX gene variant and prenatal diagnosis for a Chinese pedigree affected with X-linked hypophosphatemia]Peixuan Cao, Xiangyu Zhu, Jie Li
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 28, 2021
[Analysis of PHEX gene variant and prenatal diagnosis for a Chinese pedigree affected with X-linked hypophosphatemia]Peixuan Cao, Xiangyu Zhu, Jie Li
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 1, 2022
[Pathological variant of OFD1 gene identified in a pedigree affected with oral-facial-digital syndrome type 1]Peixuan Cao, Xiangyu Zhu, Leilei Gu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 23, 2023
[Analysis of a Chinese pedigree affected with van der Woude syndrome due to variant of IRF6 gene]Xiangyu Zhu, Peixuan Cao, Yujie Zhu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|January 29, 2023
[Value of chromosomal microarray analysis for the diagnosis of fetuses with anomalies of central nervous system]Peixuan Cao, Xiangyu Zhu, Leilei Gu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 3, 2021
[Analysis of related phenotype of prenatal cases with copy number variations in various region of 22q11.2]Peixuan Cao, Xiangyu Zhu, Leilei Gu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 14, 2018
[Mutation analysis for a methylmalonic acidemia pedigree without proband by high-throughput sequencing]Peixuan Cao, Xiangyu Zhu, Ying Yang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 9, 2022
[Analysis of PDK1 gene variants and prenatal diagnosis for eight pedigrees affected with autosomal dominant polycystic kidney disease]Huijun Li, Peixuan Cao, Xiangyu Zhu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 27, 2023
[Follow-up of fetuses with de novo copy number variations of unknown significance detected by chromosomal microarray analysis]Leilei Gu, Wei Liu, Chunxiang Zhou, et al.
BMC Pregnancy and Childbirth|July 8, 2023
Fetal congenital gastrointestinal obstruction: prenatal diagnosis of chromosome microarray analysis and pregnancy outcomesMengyao Ni, Xiangyu Zhu, Wei Liu, et al.
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