Squamous cell carcinoma of the cervix associated with choriocarcinomatous differentiation: a case report and review of the literature
Wang, Fenfen, Xu, Shanshan, Zhang, Xiaofei, Qian, Yeqing, Chen, Yaxia
Published in Journal of international medical research (01.10.2024)
Published in Journal of international medical research (01.10.2024)
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Molecular diagnostic yield of exome sequencing in a Chinese cohort of 512 fetuses with anomalies
Jin, Pengzhen, Hong, Jiawei, Xu, Yuqing, Qian, Yeqing, Han, Shuning, Dong, Minyue
Published in BMC pregnancy and childbirth (09.09.2024)
Published in BMC pregnancy and childbirth (09.09.2024)
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Case Report: Novel splicing mutations in RFX5 causing MHC class II deficiency
Chen, Shan, Xu, Yuqing, Qian, Yeqing, Li, Zhaohui, Dong, Minyue
Published in Frontiers in genetics (07.10.2022)
Published in Frontiers in genetics (07.10.2022)
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Pro-Inflammatory Signature in Decidua of Recurrent Pregnancy Loss Regardless of Embryonic Chromosomal Abnormalities
Wu, Zaigui, Wang, Miaomiao, Liang, Guanmian, Jin, Pengzhen, Wang, Peng, Xu, Yuqing, Qian, Yeqing, Jiang, Xiuxiu, Qian, Junbin, Dong, Minyue
Published in Frontiers in immunology (08.12.2021)
Published in Frontiers in immunology (08.12.2021)
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Journal Article
Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of LAMA2 gene
Xu, Yuqing, Zhu, Linyan, Qian, Yeqing, Dong, Minyue
Published in Frontiers in pediatrics (19.06.2023)
Published in Frontiers in pediatrics (19.06.2023)
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Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO)
Fan, Lihong, Jin, Pengzhen, Qian, Yeqing, Shen, Guosong, Shen, Xueping, Dong, Minyue
Published in Frontiers in genetics (22.06.2022)
Published in Frontiers in genetics (22.06.2022)
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Case Report: Prenatal diagnosis of fetal tetrasomy 9p initially identified by non-invasive prenatal testing
Yu, Jialing, Chen, Na, Chen, Min, Shen, Min, Qian, Yeqing, Dong, Minyue
Published in Frontiers in genetics (31.10.2022)
Published in Frontiers in genetics (31.10.2022)
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Case report: FOXP1 syndrome caused by a de novo splicing variant (c.1652+5 G>A) of the FOXP1 gene
Chen, Min, Sun, Yixi, Qian, Yeqing, Chen, Na, Li, Hongge, Wang, Liya, Dong, Minyue
Published in Frontiers in genetics (05.08.2022)
Published in Frontiers in genetics (05.08.2022)
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Efficiency of non-invasive prenatal screening in pregnant women at advanced maternal age
Zhu, Hui, Jin, Xiaoxiao, Xu, Yuqing, Zhang, Weihua, Liu, Xiaodan, Jin, Jinglei, Qian, Yeqing, Dong, Minyue
Published in BMC pregnancy and childbirth (26.01.2021)
Published in BMC pregnancy and childbirth (26.01.2021)
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Case report: Prenatal diagnosis of fetal intracranial hemorrhage due to compound mutations in the JAM3 gene
Xu, Min, Jin, Pengzhen, Huang, Yingzhi, Qian, Yeqing, Lin, Miaochun, Zuo, Juan, Zhu, Jin, Li, Zhaohui, Dong, Minyue
Published in Frontiers in genetics (19.10.2022)
Published in Frontiers in genetics (19.10.2022)
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Identification of four TTN variants in three families with fetal akinesia deformation sequence
Fan, Lihong, Li, Haibo, Xu, Ying, Huang, Yingzhi, Qian, Yeqing, Jin, Pengzhen, Shen, Xueping, Li, Zhi, Liu, Mingsong, Liang, Yufei, Shen, Guosong, Dong, Minyue
Published in BMC medical genomics (27.06.2024)
Published in BMC medical genomics (27.06.2024)
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circRNA-DURSA regulates trophoblast apoptosis via miR-760-HIST1H2BE axis in unexplained recurrent spontaneous abortion
Tang, Minyue, Bai, Long, Wan, Zhe, Wan, Shan, Xiang, Yu, Qian, Yeqing, Cui, Long, You, Jiali, Hu, Xiaoling, Qu, Fan, Zhu, Yimin
Published in Molecular therapy. Nucleic acids (03.12.2021)
Published in Molecular therapy. Nucleic acids (03.12.2021)
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Case Report: A Synonymous Mutation in NF1 Located at the Non-canonical Splicing Site Leading to Exon 45 Skipping
Jin, Pengzhen, Yan, Kai, Ye, Shaofen, Qian, Yeqing, Wu, Zaigui, Wang, Miaomiao, Xu, Yuqing, Xu, Yanfei, Dong, Minyue
Published in Frontiers in genetics (19.11.2021)
Published in Frontiers in genetics (19.11.2021)
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Case Report: Identification of Maternal Low-Level Mosaicism in the Dystrophin Gene by Droplet Digital Polymerase Chain Reaction
Jin, Pengzhen, Gao, Xiaoyang, Wang, Miaomiao, Qian, Yeqing, Yang, Jingjin, Yang, Yanmei, Xu, Yuqing, Xu, Yanfei, Dong, Minyue
Published in Frontiers in genetics (01.07.2021)
Published in Frontiers in genetics (01.07.2021)
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Post-implantation analysis of genomic variations in the progeny from developing fetus to birth
Zheng, Yingming, Lin, Chuanping, Wang, Wen-Jing, Wang, Liya, Qian, Yeqing, Mao, Luna, Li, Baohua, Lou, Lijun, Mao, Yuchan, Li, Na, Zheng, Jiayong, Jiang, Nan, He, Chaying, Wang, Qijing, Zhou, Qing, Chen, Fang, Jin, Fan
Published in Human genomics (15.07.2024)
Published in Human genomics (15.07.2024)
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Clinical Efficiency of Non-invasive Prenatal Screening for Common Trisomies in Low-Risk and Twin Pregnancies
Xu, Yanfei, Jin, Pengzhen, Lei, Yu, Qian, Yeqing, Xu, Yuqing, Wang, Miaomiao, Jin, Jinglei, Yin, Yixuan, Dong, Minyue
Published in Frontiers in genetics (10.05.2021)
Published in Frontiers in genetics (10.05.2021)
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Identification of a likely pathogenic structural variation in the LAMA1 gene by Bionano optical mapping
Chen, Min, Zhang, Min, Qian, Yeqing, Yang, Yanmei, Sun, Yixi, Liu, Bei, Wang, Liya, Dong, Minyue
Published in Npj genomic medicine (12.08.2020)
Published in Npj genomic medicine (12.08.2020)
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