Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center
Cai, Meiying, Lin, Na, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Xu, Shiyi, Fu, Xianguo, Xu, Liangpu, Huang, Hailong
Published in Journal of translational medicine (09.04.2022)
Published in Journal of translational medicine (09.04.2022)
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Journal Article
Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China
Cai, Meiying, Lin, Na, Guo, Nan, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, He, Shuqiong, Fu, Xianguo, Xu, Liangpu, Huang, Hailong
Published in Scientific reports (04.05.2023)
Published in Scientific reports (04.05.2023)
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Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis
Xie, Xiaorui, Huang, Baojia, Su, Linjuan, Cai, Meiying, Chen, Yuqin, Wu, Xiaoqing, Xu, Liangpu
Published in BMC medical genomics (20.11.2023)
Published in BMC medical genomics (20.11.2023)
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Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array
Cai, Meiying, Lin, Na, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, Lin, Yuan, Huang, Hailong, Xu, Liangpu
Published in Molecular biology reports (01.10.2020)
Published in Molecular biology reports (01.10.2020)
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Single Nucleotide Polymorphism array analysis for fetuses from balanced translocation carriers at the second trimester
Wu, Xiaoqing, Du, Shengrong, Liang, Bin, Su, Linjuan, Li, Ying, Chen, Yuqin, Zheng, Lin, Lin, Na, Huang, Hailong, Xu, Liangpu
Published in Heliyon (01.10.2024)
Published in Heliyon (01.10.2024)
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Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios
Wu, Xiaoqing, Li, Ying, Lin, Na, Su, Linjuan, Xie, Xiaorui, Liang, Bing, Shen, Qingmei, Cai, Meiying, Guo, Danhua, Huang, Hailong, Xu, Liangpu
Published in BMC medical genomics (30.03.2022)
Published in BMC medical genomics (30.03.2022)
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Copy number variations associated with fetal congenital kidney malformations
Cai, Meiying, Lin, Na, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, Chen, Xuemei, Lin, Yuan, Huang, Hailong, Xu, Liangpu
Published in Molecular cytogenetics (24.03.2020)
Published in Molecular cytogenetics (24.03.2020)
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Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center
Wu, Xiaoqing, Su, Linjuan, Xie, Xiaorui, He, Deqin, Chen, Xuemei, Wang, Meiying, Wang, Linshuo, Zheng, Lin, Xu, Liangpu
Published in Molecular cytogenetics (04.12.2021)
Published in Molecular cytogenetics (04.12.2021)
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Erythrocyte Indices and Hemoglobin Analysis for α-Thalassemia Screening in an Area with High Carrying Rate
Zheng, Lin, Huang, Hailong, Wu, Xiaoqing, Shen, Qingmei, Chen, Meihuan, Wang, Meiying, Su, Linjuan, Xu, Liangpu
Published in Indian journal of hematology & blood transfusion (01.04.2022)
Published in Indian journal of hematology & blood transfusion (01.04.2022)
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Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype
Su, Linjuan, Huang, Hailong, An, Gang, Cai, Meiying, Wu, Xiaoqing, Li, Ying, Xie, Xiaorui, Lin, Yuan, Wang, Meiying, Xu, Liangpu
Published in Molecular genetics & genomic medicine (01.08.2019)
Published in Molecular genetics & genomic medicine (01.08.2019)
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Chromosomal Abnormalities and Pregnancy Outcomes for Fetuses With Gastrointestinal Tract Obstructions
Wu, Xiaoqing, Su, Linjuan, Shen, Qingmei, Guo, Qun, Li, Ying, Xu, Shiyi, Lin, Na, Huang, Hailong, Xu, Liangpu
Published in Frontiers in pediatrics (06.06.2022)
Published in Frontiers in pediatrics (06.06.2022)
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Corrigendum: Chromosomal abnormalities and pregnancy outcomes for fetuses with gastrointestinal tract obstructions
Wu, Xiaoqing, Su, Linjuan, Shen, Qingmei, Guo, Qun, Li, Ying, Xu, Shiyi, Lin, Na, Huang, Hailong, Xu, Liangpu
Published in Frontiers in pediatrics (26.10.2022)
Published in Frontiers in pediatrics (26.10.2022)
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Submicroscopic aberrations of chromosome 16 in prenatal diagnosis
Wu, Xiaoqing, Xu, Liangpu, Li, Ying, Lin, Na, Su, Linjuan, Cai, Meiying, Xie, Xiaorui, Zheng, Lin, Huang, Hailong, Lin, Yuan
Published in Molecular cytogenetics (05.08.2019)
Published in Molecular cytogenetics (05.08.2019)
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Chromosomal abnormalities and copy number variations in fetal ventricular septal defects
Cai, Meiying, Huang, Hailong, Su, Linjuan, Lin, Na, Wu, Xiaoqing, Xie, Xiaorui, An, Gang, Li, Ying, Lin, Yuan, Xu, Liangpu, Cao, Hua
Published in Molecular cytogenetics (28.11.2018)
Published in Molecular cytogenetics (28.11.2018)
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Single nucleotide polymorphism array (SNP-array) analysis for fetuses with abnormal nasal bone
Xie, Xiaorui, Su, Linjuan, Li, Ying, Shen, Qingmei, Wang, Meiying, Wu, Xiaoqing
Published in Archives of gynecology and obstetrics (01.06.2024)
Published in Archives of gynecology and obstetrics (01.06.2024)
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Journal Article
Genetic evaluation for twin pregnancies using karyotyping and single nucleotide polymorphism array analysis
Wu, Xiaoqing, Huang, Baojia, Xie, Xiaorui, Cai, Meiying, Chen, Yuqin, Liang, Bin, Shen, Qingmei, Guo, Danhua, Lin, Na, Su, Linjuan, Xu, Liangpu
Published in Gene (15.02.2024)
Published in Gene (15.02.2024)
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Journal Article
Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes
Cai, Meiying, Lin, Na, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, Lin, Yuan, Xu, Liangpu, Huang, Hailong
Published in Scientific reports (15.09.2020)
Published in Scientific reports (15.09.2020)
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Journal Article
Prenatal diagnosis of Pallister‐Killian syndrome and literature review
Wu, Xiaoqing, Xie, Xiaorui, Su, Linjuan, Lin, Na, Liang, Bin, Guo, Nan, Chen, Qingquan, Xu, Liangpu, Huang, Hailong
Published in Journal of cellular and molecular medicine (01.09.2021)
Published in Journal of cellular and molecular medicine (01.09.2021)
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Journal Article
Clinical Review of Noninvasive Prenatal Testing: Experience from 551 Pregnancies with Noninvasive Prenatal Testing-Positive Results in a Tertiary Referral Center
Wu, Xiaoqing, Li, Ying, Xie, Xiaorui, Su, Linjuan, Cai, Meiying, Lin, Na, Du, Shengrong, Xu, Liangpu, Huang, Hailong
Published in The Journal of molecular diagnostics : JMD (01.12.2020)
Published in The Journal of molecular diagnostics : JMD (01.12.2020)
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Fetal mosaicism, should conventional karyotype always be performed?
Su, Linjuan, Wu, Xiaoqing, Liang, Bin, Lin, Na, Xie, Xiaorui, Cai, Meiying, Zheng, Lin, Wang, Meiying, Xu, Liangpu
Published in The journal of obstetrics and gynaecology research (01.12.2023)
Published in The journal of obstetrics and gynaecology research (01.12.2023)
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