Showing 1 - 9 results of 9 for search 'Yeqing Qian', query time: 0.03s Refine Results
  1. 1
    Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of LAMA2 gene

    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

    Published 2023-06-01
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  2. 2
    Squamous cell carcinoma of the cervix associated with choriocarcinomatous differentiation: a case report and review of the literature

    Squamous cell carcinoma of the cervix associated with choriocarcinomatous differentiation: a case report and review of the literature by Fenfen Wang, Shanshan Xu, Xiaofei Zhang, Yeqing Qian, Yaxia Chen

    Published 2024-10-01
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  3. 3
    Molecular diagnostic yield of exome sequencing in a Chinese cohort of 512 fetuses with anomalies

    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

    Published 2024-09-01
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  4. 4
    Case Report: Prenatal diagnosis of fetal tetrasomy 9p initially identified by non-invasive prenatal testing

    Case Report: Prenatal diagnosis of fetal tetrasomy 9p initially identified by non-invasive prenatal testing by Jialing Yu, Na Chen, Min Chen, Min Shen, Yeqing Qian, Minyue Dong, Minyue Dong, Minyue Dong

    Published 2022-10-01
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  5. 5
    Synonymous variant at the terminal nucleotide in exon 3 of F7 causes abnormal splicing: A case report

    Synonymous variant at the terminal nucleotide in exon 3 of F7 causes abnormal splicing: A case report by Liya Wang, Wenshan Zeng, Yeqing Qian, Yixi Sun, Min Chen, Bei Liu, Junjie Hu, Ping Yu, Minyue Dong

    Published 2024-07-01
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  6. 6
    Identification of four TTN variants in three families with fetal akinesia deformation sequence

    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

    Published 2024-06-01
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  7. 7
    Fine-tuning of Wnt signaling by RNA surveillance factor Smg5 in the mouse craniofacial development

    Fine-tuning of Wnt signaling by RNA surveillance factor Smg5 in the mouse craniofacial development by Shicheng Zhu, Suman Huo, Weiran He, Caiyan Huang, Jiannan Zhang, Xiaoning Jiang, Yeqing Qian, Chengyan Chen, Zhong-Min Dai, Xueqin Yang, Mengsheng Qiu, Tangliang Li, Xiao-Jing Zhu

    Published 2025-03-01
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  8. 8
    Post-implantation analysis of genomic variations in the progeny from developing fetus to birth

    Post-implantation analysis of genomic variations in the progeny from developing fetus to birth by Yingming Zheng, Chuanping Lin, Wen-Jing Wang, Liya Wang, Yeqing Qian, Luna Mao, Baohua Li, Lijun Lou, Yuchan Mao, Na Li, Jiayong Zheng, Nan Jiang, Chaying He, Qijing Wang, Qing Zhou, Fang Chen, Fan Jin

    Published 2024-07-01
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  9. 9
    Validation and depth evaluation of recurrent neural network‐based ultra low‐pass genome sequencing for the detection of absence of heterozygosity: A multi‐centre study of 409 cases

    Validation and depth evaluation of recurrent neural network‐based ultra low‐pass genome sequencing for the detection of absence of heterozygosity: A multi‐centre study of 409 cases... by Yeqing Qian, Jianjun Zhu, Zhiguo Tang, Yan Sun, Zhonghua Wang, Fei Tang, Yun Yang, Linlin Fan, Yixi Sun, Bei Liu, Min Chen, Yuqin Luo, Junjie Hu, Kai Yan, Jianfen Man, Lina Wang, Cangcang Jia, Ping Tang, Xinyi Zhu, Chaohong Wang, Junxiang Tang, Yuanyuan Xia, Xueqin Guo, Kang Zhang, Xiaoli Wang, Suping Li, Lijie Song, Jiansheng Zhu, Minyue Dong

    Published 2024-07-01
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