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Meiying Cai

Showing results (31-40 of 79) with videos related to

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BMC Women'S Health|October 22, 2025
Association between high-density lipoprotein cholesterol-related inflammatory markers and female infertility: a cross-sectional analysis from the National Health and Nutrition Examination Survey (NHANES 2013-2018)Siqi Cao, Meiying Cai, Haimei Zhang, et al.
BMC Medical Genomics|August 23, 2023
Genetic and ultrasonographic analyses of fetuses with 1q21.1q21.2 microdeletion/microduplication: a retrospective studyNan Guo, Huili Xue, Bin Liang, et al.
BMC Medical Genomics|January 13, 2021
Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markersMeiying Cai, Na Lin, Xuemei Chen, et al.
Risk Management and Healthcare Policy|June 24, 2021
Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical OutcomesMeiying Cai, Hailong Huang, Linjuan Su, et al.
Journal of Cellular and Molecular Medicine|July 4, 2023
Pathogenic copy number variations are associated with foetal short femur length in a tertiary referral centre studyMeiying Cai, Yanting Que, Meihuan Chen, et al.
Frontiers in Pediatrics|August 29, 2022
Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndromeMeiying Cai, Min Lin, Nan Guo, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 12, 2017
[Prenatal diagnosis of 22q11 microdeletion syndrome]Meiying Cai, Hailong Huang, Na Lin, et al.
BMC Medical Genomics|November 21, 2023
Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysisXiaorui Xie, Baojia Huang, Linjuan Su, et al.
Molecular Genetics & Genomic Medicine|April 26, 2025
Ultrasound Phenotype, Genetic Analysis, and Pregnancy Outcomes of Fetuses With 1p36 Deletion SyndromeMeiying Cai, Na Lin, Xuemei Chen, et al.
Diagnostics (Basel, Switzerland)|March 28, 2026
Spectrum of Copy Number Variants in Fetal Congenital Heart Disease and Their Clinical Implications: A Retrospective Study from a Tertiary Care CenterMeiying Cai, Na Lin, Meimei Fu, et al.
Pageof 8

Showing results (31-40 of 79) with videos related to

Sort By:
Pageof 8
BMC Women'S Health|October 22, 2025
Association between high-density lipoprotein cholesterol-related inflammatory markers and female infertility: a cross-sectional analysis from the National Health and Nutrition Examination Survey (NHANES 2013-2018)Siqi Cao, Meiying Cai, Haimei Zhang, et al.
BMC Medical Genomics|August 23, 2023
Genetic and ultrasonographic analyses of fetuses with 1q21.1q21.2 microdeletion/microduplication: a retrospective studyNan Guo, Huili Xue, Bin Liang, et al.
BMC Medical Genomics|January 13, 2021
Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markersMeiying Cai, Na Lin, Xuemei Chen, et al.
Risk Management and Healthcare Policy|June 24, 2021
Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical OutcomesMeiying Cai, Hailong Huang, Linjuan Su, et al.
Journal of Cellular and Molecular Medicine|July 4, 2023
Pathogenic copy number variations are associated with foetal short femur length in a tertiary referral centre studyMeiying Cai, Yanting Que, Meihuan Chen, et al.
Frontiers in Pediatrics|August 29, 2022
Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndromeMeiying Cai, Min Lin, Nan Guo, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 12, 2017
[Prenatal diagnosis of 22q11 microdeletion syndrome]Meiying Cai, Hailong Huang, Na Lin, et al.
BMC Medical Genomics|November 21, 2023
Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysisXiaorui Xie, Baojia Huang, Linjuan Su, et al.
Molecular Genetics & Genomic Medicine|April 26, 2025
Ultrasound Phenotype, Genetic Analysis, and Pregnancy Outcomes of Fetuses With 1p36 Deletion SyndromeMeiying Cai, Na Lin, Xuemei Chen, et al.
Diagnostics (Basel, Switzerland)|March 28, 2026
Spectrum of Copy Number Variants in Fetal Congenital Heart Disease and Their Clinical Implications: A Retrospective Study from a Tertiary Care CenterMeiying Cai, Na Lin, Meimei Fu, et al.
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