Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis

por Xie, Xiaorui, Huang, Baojia, Su, Linjuan, Cai, Meiying, Chen, Yuqin, Wu, Xiaoqing, Xu, Liangpu
Publicado 2023

Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical Outcomes

por Cai, Meiying, Huang, Hailong, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Xu, Liangpu, Lin, Na
Publicado 2021

Application of Single Nucleotide Polymorphism Microarray in Prenatal Diagnosis of Fetuses with Central Nervous System Abnormalities

por Xie, Xiaorui, Wu, Xiaoqing, Su, Linjuan, Cai, Meiying, Li, Ying, Huang, Hailong, Xu, Liangpu
Publicado 2021

Screening of Some Indicators for Alpha-Thalassemia in Fujian Province of Southern China

por Zheng, Lin, Huang, Hailong, Wu, Xiaoqing, Su, Linjuan, Shen, Qingmei, Wang, Meiying, Lin, Na, Xu, Liangpu
Publicado 2021

Different Cutoff Values for Increased Nuchal Translucency in First-Trimester Screening to Predict Fetal Chromosomal Abnormalities

por Su, Linjuan, Wu, Xiaoqing, Lin, Na, Xie, Xiaorui, Cai, Meiying, Wang, Meiying, Zheng, Lin, Xu, Liangpu
Publicado 2021

Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes

por Cai, Meiying, Lin, Na, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, Lin, Yuan, Xu, Liangpu, Huang, Hailong
Publicado 2020

Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype

por Wu, Xiaoqing, Li, Ying, Su, Linjuan, Xie, Xiaorui, Cai, Meiying, Lin, Na, Huang, Hailong, Lin, Yuan, Xu, Liangpu
Publicado 2020

Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array

por Cai, Meiying, Lin, Na, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, Lin, Yuan, Huang, Hailong, Xu, Liangpu
Publicado 2020

Prenatal diagnosis of Pallister‐Killian syndrome and literature review

por Wu, Xiaoqing, Xie, Xiaorui, Su, Linjuan, Lin, Na, Liang, Bin, Guo, Nan, Chen, Qingquan, Xu, Liangpu, Huang, Hailong
Publicado 2021

Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center

por Wu, Xiaoqing, Su, Linjuan, Xie, Xiaorui, He, Deqin, Chen, Xuemei, Wang, Meiying, Wang, Linshuo, Zheng, Lin, Xu, Liangpu
Publicado 2021

Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center

por Cai, Meiying, Lin, Na, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Xu, Shiyi, Fu, Xianguo, Xu, Liangpu, Huang, Hailong
Publicado 2022

Chromosomal Abnormalities and Pregnancy Outcomes for Fetuses With Gastrointestinal Tract Obstructions

por Wu, Xiaoqing, Su, Linjuan, Shen, Qingmei, Guo, Qun, Li, Ying, Xu, Shiyi, Lin, Na, Huang, Hailong, Xu, Liangpu
Publicado 2022

Corrigendum: Chromosomal abnormalities and pregnancy outcomes for fetuses with gastrointestinal tract obstructions

por Wu, Xiaoqing, Su, Linjuan, Shen, Qingmei, Guo, Qun, Li, Ying, Xu, Shiyi, Lin, Na, Huang, Hailong, Xu, Liangpu
Publicado 2022

Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome

por Cai, Meiying, Huang, Hailong, Su, Linjuan, Lin, Na, Wu, Xiaoqing, Xie, Xiaorui, An, Gang, Li, Ying, Lin, Yuan, Xu, Liangpu
Publicado 2018

Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype

por Su, Linjuan, Huang, Hailong, An, Gang, Cai, Meiying, Wu, Xiaoqing, Li, Ying, Xie, Xiaorui, Lin, Yuan, Wang, Meiying, Xu, Liangpu
Publicado 2019

Submicroscopic aberrations of chromosome 16 in prenatal diagnosis

por Wu, Xiaoqing, Xu, Liangpu, Li, Ying, Lin, Na, Su, Linjuan, Cai, Meiying, Xie, Xiaorui, Zheng, Lin, Huang, Hailong, Lin, Yuan
Publicado 2019

Copy number variations associated with fetal congenital kidney malformations

por Cai, Meiying, Lin, Na, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, Chen, Xuemei, Lin, Yuan, Huang, Hailong, Xu, Liangpu
Publicado 2020

Chromosomal abnormalities and copy number variations in fetal ventricular septal defects

por Cai, Meiying, Huang, Hailong, Su, Linjuan, Lin, Na, Wu, Xiaoqing, Xie, Xiaorui, An, Gang, Li, Ying, Lin, Yuan, Xu, Liangpu, Cao, Hua
Publicado 2018

Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China

por Cai, Meiying, Lin, Na, Guo, Nan, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, He, Shuqiong, Fu, Xianguo, Xu, Liangpu, Huang, Hailong
Publicado 2023

Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arrays

por Cai, Meiying, Lin, Na, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, Chen, Xuemei, Dai, Yifang, Lin, Yuan, Huang, Hailong, Xu, Liangpu
Publicado 2019