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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
January 25, 2022
[Prenatal ultrasonographic manifestations and genetic analysis of eight fetuses with 16p11.2 microdeletions]
Meiying Cai, Hailong Huang, Na Lin, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
May 20, 2023
Classifying and evaluating fetuses with multicystic dysplastic kidney in etiologic studies
Meiying Cai, Chong Guo, Xinrui Wang, et al.
Experimental and Therapeutic Medicine
|
June 29, 2023
Molecular genetic analysis of 1,980 cases of male infertility
Meimei Fu, Meihuan Chen, Nan Guo, et al.
Journal of Translational Medicine
|
April 10, 2022
Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center
Meiying Cai, Na Lin, Linjuan Su, et al.
Molecular Diagnosis & Therapy
|
July 12, 2020
Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype
Xiaoqing Wu, Ying Li, Linjuan Su, et al.
BMC Pregnancy and Childbirth
|
October 11, 2025
Detection of chromosomal and gene abnormality with karyotyping, chromosomal microarray analysis and trio-based whole exome sequencing in pregnancies with fetal growth restriction: implications for precise prenatal diagnosis
Yangping Chen, Meiying Cai, Meihuan Chen, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
June 28, 2023
Non-invasive prenatal testing for the diagnosis of congenital abnormalities: Insights from a large multicenter study in southern China
Meiying Cai, Na Lin, Xuemei Chen, et al.
Archives of Gynecology and Obstetrics
|
November 4, 2025
Can cell-free fetal DNA screening be utilized for the assessment of chromosomal abnormalities in fetuses with mildly increased nuchal translucency?
Linjuan Su, Wantong Zhao, Hailong Huang, et al.
Scientific Reports
|
September 16, 2020
Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes
Meiying Cai, Na Lin, Linjuan Su, et al.
Molecular Biology Reports
|
September 16, 2020
Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array
Meiying Cai, Na Lin, Linjuan Su, et al.
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Showing results (51-60 of 79) with videos related to
Sort By:
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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
January 25, 2022
[Prenatal ultrasonographic manifestations and genetic analysis of eight fetuses with 16p11.2 microdeletions]
Meiying Cai, Hailong Huang, Na Lin, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
May 20, 2023
Classifying and evaluating fetuses with multicystic dysplastic kidney in etiologic studies
Meiying Cai, Chong Guo, Xinrui Wang, et al.
Experimental and Therapeutic Medicine
|
June 29, 2023
Molecular genetic analysis of 1,980 cases of male infertility
Meimei Fu, Meihuan Chen, Nan Guo, et al.
Journal of Translational Medicine
|
April 10, 2022
Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center
Meiying Cai, Na Lin, Linjuan Su, et al.
Molecular Diagnosis & Therapy
|
July 12, 2020
Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype
Xiaoqing Wu, Ying Li, Linjuan Su, et al.
BMC Pregnancy and Childbirth
|
October 11, 2025
Detection of chromosomal and gene abnormality with karyotyping, chromosomal microarray analysis and trio-based whole exome sequencing in pregnancies with fetal growth restriction: implications for precise prenatal diagnosis
Yangping Chen, Meiying Cai, Meihuan Chen, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
June 28, 2023
Non-invasive prenatal testing for the diagnosis of congenital abnormalities: Insights from a large multicenter study in southern China
Meiying Cai, Na Lin, Xuemei Chen, et al.
Archives of Gynecology and Obstetrics
|
November 4, 2025
Can cell-free fetal DNA screening be utilized for the assessment of chromosomal abnormalities in fetuses with mildly increased nuchal translucency?
Linjuan Su, Wantong Zhao, Hailong Huang, et al.
Scientific Reports
|
September 16, 2020
Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes
Meiying Cai, Na Lin, Linjuan Su, et al.
Molecular Biology Reports
|
September 16, 2020
Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array
Meiying Cai, Na Lin, Linjuan Su, et al.
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of 8