Genetic and ultrasonographic analyses of fetuses with 1q21.1q21.2 microdeletion/microduplication: a retrospective study

por Guo, Nan, Xue, Huili, Liang, Bin, Huang, Hailong, Cai, Meiying, Xu, Liangpu
Publicado 2023

Positive predictive value of noninvasive prenatal testing for sex chromosome abnormalities

por Guo, Nan, Cai, Meiying, Lin, Min, Xue, Huili, Huang, Hailong, Xu, Liangpu
Publicado 2022

Molecular cytogenetic identification of small supernumerary marker chromosomes using chromosome microarray analysis

por Xue, Huili, Huang, Hailong, Wang, Yan, An, Gang, Zhang, Min, Xu, Liangpu, Lin, Yuan
Publicado 2019

Vaginal Microbiota Diversity of Patients with Embryonic Miscarriage by Using 16S rDNA High-Throughput Sequencing

por Xu, Linfen, Huang, Lingna, Lian, Chengying, Xue, Huili, Lu, Yanfang, Chen, Xiujuan, Xia, Yong
Publicado 2020

Prenatal diagnosis of PLP1 duplication by single nucleotide polymorphism array in a family with Pelizaeus-Merzbacher disease

por Xue, Huili, Yu, Aili, Chen, Xuemei, Lin, Na, Lin, Min, Huang, Hailong, Xu, Liangpu
Publicado 2021

Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis

por Xue, Huili, Chen, Xuemei, Lin, Min, Lin, Na, Huang, Hailong, Yu, Aili, Xu, Liangpu
Publicado 2020

Performance of Chromosomal Microarray Analysis for Detection of Copy Number Variations in Fetal Echogenic Bowel

por Fan, Xiangqun, Huang, Hailong, Lin, Xiyao, Xue, Huili, Cai, Meiying, Lin, Na, Xu, Liangpu
Publicado 2021

Efficiency of expanded noninvasive prenatal testing in the detection of fetal subchromosomal microdeletion and microduplication in a cohort of 31,256 single pregnancies

por Xue, Huili, Yu, Aili, Lin, Min, Chen, Xuemei, Guo, Qun, Xu, Liangpu, Huang, Hailong
Publicado 2022

Prenatal genetic analysis of fetal aberrant right subclavian artery with or without additional ultrasound anomalies in a third level referral center

por Xue, Huili, Zhang, Lin, Yu, Aili, Lin, Min, Guo, Qun, Xu, Liangpu, Huang, Hailong
Publicado 2023

Detection of copy number variation associated with ventriculomegaly in fetuses using single nucleotide polymorphism arrays

por Xue, Huili, Yu, Aili, Lin, Na, Chen, Xuemei, Lin, Min, Wang, Yan, Huang, Hailong, Xu, Liangpu
Publicado 2021

Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China

por Huang, Hailong, Xu, Liangpu, Chen, Meihuan, Lin, Na, Xue, Huili, Chen, Lingji, Wang, Yan, He, Deqin, Zhang, Min, Lin, Yuan
Publicado 2019

Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy

por Mao, Bin, Lin, Na, Guo, Danhua, He, Deqin, Xue, Huili, Chen, Lingji, He, Qianqian, Zhang, Min, Chen, Meihuan, Huang, Hailong, Xu, Liangpu
Publicado 2023