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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
December 1, 2022
[Ultrasonographic phenotype and genetic analysis of fetuses with 17q12 microdeletion]
Meiying Cai, Hailong Huang, Linjuan Su, et al.
International Journal of General Medicine
|
November 5, 2021
Screening of Some Indicators for Alpha-Thalassemia in Fujian Province of Southern China
Lin Zheng, Hailong Huang, Xiaoqing Wu, et al.
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.
Plos One
|
August 4, 2025
Hematological analysis of alpha-thalassemia: A single-center, retrospective clinical study
Lin Zheng, Nuolan Yin, Meiying Wang, et al.
Frontiers in Pediatrics
|
July 5, 2022
Chromosomal Abnormalities and Pregnancy Outcomes for Fetuses With Gastrointestinal Tract Obstructions
Xiaoqing Wu, Linjuan Su, Qingmei Shen, 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.
The Journal of Obstetrics and Gynaecology Research
|
October 16, 2023
Fetal mosaicism, should conventional karyotype always be performed?
Linjuan Su, Xiaoqing Wu, Bin Liang, 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.
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.
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Showing results (11-20 of 39) with videos related to
Sort By:
Page
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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
December 1, 2022
[Ultrasonographic phenotype and genetic analysis of fetuses with 17q12 microdeletion]
Meiying Cai, Hailong Huang, Linjuan Su, et al.
International Journal of General Medicine
|
November 5, 2021
Screening of Some Indicators for Alpha-Thalassemia in Fujian Province of Southern China
Lin Zheng, Hailong Huang, Xiaoqing Wu, et al.
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.
Plos One
|
August 4, 2025
Hematological analysis of alpha-thalassemia: A single-center, retrospective clinical study
Lin Zheng, Nuolan Yin, Meiying Wang, et al.
Frontiers in Pediatrics
|
July 5, 2022
Chromosomal Abnormalities and Pregnancy Outcomes for Fetuses With Gastrointestinal Tract Obstructions
Xiaoqing Wu, Linjuan Su, Qingmei Shen, 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.
The Journal of Obstetrics and Gynaecology Research
|
October 16, 2023
Fetal mosaicism, should conventional karyotype always be performed?
Linjuan Su, Xiaoqing Wu, Bin Liang, 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.
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.
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of 4