Hasil Pencarian - Meiying Cai

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  1. 1
    Classifying and Evaluating Fetuses With Ventriculomegaly in Genetic Etiologic Studies

    Classifying and Evaluating Fetuses With Ventriculomegaly in Genetic Etiologic Studies oleh Meiying Cai, Hailong Huang, Liangpu Xu, Na Lin

    Diterbitkan 2021-07-01
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  2. 2
    Clinical Utility and the Yield of Single Nucleotide Polymorphism Array in Prenatal Diagnosis of Fetal Central Nervous System Abnormalities

    Clinical Utility and the Yield of Single Nucleotide Polymorphism Array in Prenatal Diagnosis of Fetal Central Nervous System Abnormalities oleh Meiying Cai, Hailong Huang, Liangpu Xu, Na Lin

    Diterbitkan 2021-05-01
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  3. 3
    Prenatal Diagnosis of 17p11.2 Copy Number Abnormalities Associated With Smith–Magenis and Potocki–Lupski Syndromes in Fetuses

    Prenatal Diagnosis of 17p11.2 Copy Number Abnormalities Associated With Smith–Magenis and Potocki–Lupski Syndromes in Fetuses oleh Meiying Cai, Xianguo Fu, Liangpu Xu, Na Lin, Hailong Huang

    Diterbitkan 2021-12-01
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  4. 4
    Genetic and ultrasonographic analyses of fetuses with 1q21.1q21.2 microdeletion/microduplication: a retrospective study

    Genetic and ultrasonographic analyses of fetuses with 1q21.1q21.2 microdeletion/microduplication: a retrospective study oleh Nan Guo, Huili Xue, Bin Liang, Hailong Huang, Meiying Cai, Liangpu Xu

    Diterbitkan 2023-08-01
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  5. 5
    Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study

    Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective c... oleh Meiying Cai, Aixiang Lv, Wantong Zhao, Liangpu Xu, Na Lin, Hailong Huang

    Diterbitkan 2024-01-01
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  6. 6
    Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndrome

    Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndrome oleh Meiying Cai, Min Lin, Nan Guo, Meimei Fu, Liangpu Xu, Na Lin, Hailong Huang

    Diterbitkan 2022-08-01
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  7. 7
    Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis

    Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis oleh Xiaorui Xie, Baojia Huang, Linjuan Su, Meiying Cai, Yuqin Chen, Xiaoqing Wu, Liangpu Xu

    Diterbitkan 2023-11-01
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  8. 8
    Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers

    Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers oleh Meiying Cai, Na Lin, Xuemei Chen, Meimei Fu, Nan Guo, Liangpu Xu, Hailong Huang

    Diterbitkan 2021-01-01
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  9. 9
    16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up

    16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up oleh Meiying Cai, Yanting Que, Xuemei Chen, Yuqing Chen, Bin Liang, Hailong Huang, Liangpu Xu, Na Lin

    Diterbitkan 2022-12-01
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  10. 10
    Fetal Aberrant Right Subclavian Artery: Associated Anomalies, Genetic Etiology, and Postnatal Outcomes in a Retrospective Cohort Study

    Fetal Aberrant Right Subclavian Artery: Associated Anomalies, Genetic Etiology, and Postnatal Outcomes in a Retrospective Cohort Study oleh Meiying Cai, Na Lin, Xiangqun Fan, Xuemei Chen, Shiyi Xu, Xianguo Fu, Liangpu Xu, Hailong Huang

    Diterbitkan 2022-06-01
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  11. 11
    Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center

    Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center oleh Meiying Cai, Na Lin, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Shiyi Xu, Xianguo Fu, Liangpu Xu, Hailong Huang

    Diterbitkan 2022-04-01
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  12. 12
    Non-invasive prenatal testing for the diagnosis of congenital abnormalities: Insights from a large multicenter study in southern China

    Non-invasive prenatal testing for the diagnosis of congenital abnormalities: Insights from a large multicenter study in southern China oleh Meiying Cai, Na Lin, Xuemei Chen, Ying Li, Min Lin, Xianguo Fu, Hailong Huang, Shuqiong He, Liangpu Xu

    Diterbitkan 2023-06-01
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  13. 13
    Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype

    Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype oleh Linjuan Su, Hailong Huang, Gang An, Meiying Cai, Xiaoqing Wu, Ying Li, Xiaorui Xie, Yuan Lin, Meiying Wang, Liangpu Xu

    Diterbitkan 2019-08-01
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  14. 14
    Submicroscopic aberrations of chromosome 16 in prenatal diagnosis

    Submicroscopic aberrations of chromosome 16 in prenatal diagnosis oleh Xiaoqing Wu, Liangpu Xu, Ying Li, Na Lin, Linjuan Su, Meiying Cai, Xiaorui Xie, Lin Zheng, Hailong Huang, Yuan Lin

    Diterbitkan 2019-08-01
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  15. 15
    Prenatal diagnosis of genetic aberrations in fetuses with pulmonary stenosis in southern China: a retrospective analysis

    Prenatal diagnosis of genetic aberrations in fetuses with pulmonary stenosis in southern China: a retrospective analysis oleh Meiying Cai, Nan Guo, Meimei Fu, Yuqing Chen, Bin Liang, Yanting Que, Qingqiang Ji, Hailong Huang, Liangpu Xu, Na Lin

    Diterbitkan 2023-05-01
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  16. 16
    Copy number variations associated with fetal congenital kidney malformations

    Copy number variations associated with fetal congenital kidney malformations oleh Meiying Cai, Na Lin, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Ying Li, Xuemei Chen, Yuan Lin, Hailong Huang, Liangpu Xu

    Diterbitkan 2020-03-01
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  17. 17
    Chromosomal abnormalities and copy number variations in fetal ventricular septal defects

    Chromosomal abnormalities and copy number variations in fetal ventricular septal defects oleh Meiying Cai, Hailong Huang, Linjuan Su, Na Lin, Xiaoqing Wu, Xiaorui Xie, Gang An, Ying Li, Yuan Lin, Liangpu Xu, Hua Cao

    Diterbitkan 2018-11-01
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  18. 18
    Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China

    Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China oleh Meiying Cai, Na Lin, Nan Guo, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Ying Li, Shuqiong He, Xianguo Fu, Liangpu Xu, Hailong Huang

    Diterbitkan 2023-05-01
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  19. 19
    Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele in China: a single tertiary center study

    Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele in China: a single tertiary center study oleh Yanting Que, Meiying Cai, Fang Yang, Qingqiang Ji, Shuqi Zhang, Wenhui Huang, Yashi Gao, Bojing Zhou, Hailong Huang, Hua Cao, Na Lin

    Diterbitkan 2023-09-01
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  20. 20
    Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios

    Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios oleh Xiaoqing Wu, Ying Li, Na Lin, Linjuan Su, Xiaorui Xie, Bing Liang, Qingmei Shen, Meiying Cai, Danhua Guo, Hailong Huang, Liangpu Xu

    Diterbitkan 2022-03-01
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