Hasil Pencarian - Xiangyi Jing

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  1. 1
    PDIA2 variant associated with vitiligo

    PDIA2 variant associated with vitiligo oleh Fucheng Li, Can Liao, Ru Li, Yongling Zhang, Xiangyi Jing, Dongzhi Li, Weiping Deng

    Diterbitkan 2023-10-01
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  2. 2
    Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China

    Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China oleh Rongyue Wang, Tingying Lei, Fang Fu, Ru Li, Xiangyi Jing, Xin Yang, Juan Liu, Dongzhi Li, Can Liao

    Diterbitkan 2019-02-01
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  3. 3
    Prenatal diagnosis of ultrasound soft markers in a single medical center of mainland China

    Prenatal diagnosis of ultrasound soft markers in a single medical center of mainland China oleh Yanhong Zhou, Siqi Wu, Jin Han, Li Zhen, Xin Yang, Ru Li, Yongling Zhang, Xiangyi Jing, Fucheng Li, Huishu Liu

    Diterbitkan 2023-02-01
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  4. 4
    Variant spectrum of F8 and F9 in hemophilia patients from southern China and 26 novel variants

    Variant spectrum of F8 and F9 in hemophilia patients from southern China and 26 novel variants oleh Fucheng Li, Liya He, Guilan Chen, Yan Lu, Ru Li, Yongling Zhang, Xiangyi Jing, Rujuan Ling, Dongzhi Li, Can Liao

    Diterbitkan 2023-12-01
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  5. 5
    The Genetic and Clinical Outcomes in Fetuses With Isolated Fetal Growth Restriction: A Chinese Single-Center Retrospective Study

    The Genetic and Clinical Outcomes in Fetuses With Isolated Fetal Growth Restriction: A Chinese Single-Center Retrospective Study oleh Hang Zhou, Ken Cheng, Yingsi Li, Fang Fu, Ru Li, Yongling Zhang, Xin Yang, Xiangyi Jing, Fucheng Li, Jin Han, Min Pan, Li Zhen, Dongzhi Li, Can Liao

    Diterbitkan 2022-04-01
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  6. 6
    Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis

    Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis oleh Ruibin Huang, Hang Zhou, Fang Fu, Ru Li, Tingying Lei, Yingsi Li, Ken Cheng, You Wang, Xin Yang, Lushan Li, Xiangyi Jing, Yongling Zhang, Fucheng Li, Dongzhi Li, Can Liao

    Diterbitkan 2022-06-01
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  7. 7
    Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing

    Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing oleh Fang Fu, Fang Fu, Ru Li, Xiao Dang, Qiuxia Yu, Ke Xu, Weiyue Gu, Dan Wang, Xin Yang, Min Pan, Li Zhen, Yongling Zhang, Fatao Li, Xiangyi Jing, Fucheng Li, Dongzhi Li, Can Liao

    Diterbitkan 2022-09-01
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  8. 8
    Prenatal diagnosis in fetal right aortic arch using chromosomal microarray analysis and whole exome sequencing: a Chinese single-center retrospective study

    Prenatal diagnosis in fetal right aortic arch using chromosomal microarray analysis and whole exome sequencing: a Chinese single-center retrospective study oleh Lu Zhang, Ruibin Huang, Hang Zhou, Xiaomei Lin, Fei Guo, Xiangyi Jing, Yongling Zhang, Fucheng Li, Fatao Li, Qiuxia Yu, Dan Wang, Guilan Chen, Fang Fu, Min Pan, Jin Han, Dongzhi Li, Ru Li

    Diterbitkan 2024-09-01
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  9. 9
    A Deep-Learning-Based Method Can Detect Both Common and Rare Genetic Disorders in Fetal Ultrasound

    A Deep-Learning-Based Method Can Detect Both Common and Rare Genetic Disorders in Fetal Ultrasound oleh Jiajie Tang, Jin Han, Jiaxin Xue, Li Zhen, Xin Yang, Min Pan, Lianting Hu, Ru Li, Yuxuan Jiang, Yongling Zhang, Xiangyi Jing, Fucheng Li, Guilian Chen, Kanghui Zhang, Fanfan Zhu, Can Liao, Long Lu

    Diterbitkan 2023-06-01
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  10. 10
    Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature review

    Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature review oleh Ruibin Huang, Chunling Ma, Huanyi Chen, Fang Fu, Jin Han, Liyuan Liu, Lushan Li, Shujuan Yan, Jianqin Lu, Hang Zhou, You Wang, Fei Guo, Xiangyi Jing, Fucheng Li, Li Zhen, Dongzhi Li, Ru Li, Can Liao

    Diterbitkan 2024-09-01
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  11. 11
    Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses

    Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses oleh Fang Fu, Ru Li, Qiuxia Yu, Dan Wang, Qiong Deng, Lushan Li, Tingying Lei, Guilan Chen, Zhiqiang Nie, Xin Yang, Jin Han, Min Pan, Li Zhen, Yongling Zhang, Xiangyi Jing, Fucheng Li, Fatao Li, Lina Zhang, Cuixing Yi, Yingsi Li, Yan Lu, Hang Zhou, Ken Cheng, Jian Li, Lina Xiang, Jing Zhang, Sha Tang, Ping Fang, Dongzhi Li, Can Liao

    Diterbitkan 2022-10-01
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