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

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

Xiaorui Xie, Xiaoqing Wu, Linjuan Su, Meiying Cai, Ying Li, Hailong Huang, Liangpu Xu Medical Genetic Diagnosis and Therapy Center, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fujian Provincial Maternity and Children’s Hospital, Affiliated Hospital of Fujian Medical University, Fu...

Full description

Bibliographic Details
Main Authors:	Xie X, Wu X, Su L, Cai M, Li Y, Huang H, Xu L
Format:	Article
Language:	English
Published:	Dove Medical Press 2021-08-01
Series:	International Journal of General Medicine
Subjects:	central nervous system abnormalities chromosome karyotype analysis single nucleotide polymorphism microarray prenatal diagnosis
Online Access:	https://www.dovepress.com/application-of-single-nucleotide-polymorphism-microarray-in-prenatal-d-peer-reviewed-fulltext-article-IJGM

Similar Items

Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities
by: Shanning Wan, et al.
Published: (2019-05-01)

Application of chromosome microarray analysis in prenatal diagnosis
by: Mingjing Xia, et al.
Published: (2020-11-01)

Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype
by: Linjuan Su, et al.
Published: (2019-08-01)

Potentials and challenges of chromosomal microarray analysis in prenatal diagnosis
by: Xijing Liu, et al.
Published: (2022-07-01)

Application of Chromosome Microarray in Diagnosis of Amniotic Fluid in Older Pregnant Women
by: Guangting Lu, et al.
Published: (2023-07-01)

Prenatal diagnosis of fetuses conceived by assisted reproductive technology by karyotyping and chromosomal microarray analysis
by: Huan Guo, et al.
Published: (2023-01-01)

Comparison of Chromosomal Microarray Analysis and Noninvasive Prenatal Testing in Pregnant Women with Fetal Ultrasonic Soft Markers
by: Hu X, et al.
Published: (2024-01-01)

Conventional Chromosome Analysis of Fetuses with Central Nervous System Anomalies and Associated Anomalies: Is Anything Changed?
by: Emre Ekmekci, et al.
Published: (2018-02-01)

The use of chromosomal microarray analysis for diagnostics of chromosomal pathology in fetal central nervous system malformations
by: J. K. Kievskaya, et al.
Published: (2020-10-01)

Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing
by: Xiaomei Shi, et al.
Published: (2021-01-01)

Retrospective analysis of the sex chromosomal copy number variations in 186 fetuses using single nucleotide polymorphism arrays
by: Haiwei Wang, et al.
Published: (2022-12-01)

Isolated Increased Nuchal Translucency in First Trimester Ultrasound Scan: Diagnostic Yield of Prenatal Microarray and Outcome of Pregnancy
by: Kyra E. Stuurman, et al.
Published: (2021-10-01)

Chromosomal Abnormalities and Pregnancy Outcomes for Fetuses With Gastrointestinal Tract Obstructions
by: Xiaoqing Wu, et al.
Published: (2022-06-01)

Clinical experience of noninvasive prenatal testing for rare chromosome abnormalities in singleton pregnancies
by: Ting Hu, et al.
Published: (2022-09-01)

Corrigendum: Chromosomal abnormalities and pregnancy outcomes for fetuses with gastrointestinal tract obstructions
by: Xiaoqing Wu, et al.
Published: (2022-10-01)

The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray Analysis
by: Yu'e Chen, et al.
Published: (2021-10-01)

Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong
by: Claudia Ching Yan Chung, et al.
Published: (2020-02-01)

Cytogenetic Analysis of Amniotic Fluid Cells in 4206 Cases of High-Risk Pregnant Women
by: Huafeng LI, et al.
Published: (2019-01-01)

Application of chromosome microarray analysis and karyotyping in diagnostic assessment of abnormal Down syndrome screening results
by: Han Kang, et al.
Published: (2022-11-01)

Diagnostic cytogenetic testing following positive noninvasive prenatal screening results of sex chromosome abnormalities: Report of five cases and systematic review of evidence
by: Xiaolei Xie, et al.
Published: (2020-07-01)

Chromosomal microarray analysis in fetuses with high-risk prenatal indications: A retrospective study in China
by: Xiaomei Luo, et al.
Published: (2021-03-01)

Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis
by: Xiaorui Xie, et al.
Published: (2023-11-01)

Clinical application of chromosomal microarray analysis for fetuses with craniofacial malformations
by: Chenyang Xu, et al.
Published: (2020-08-01)

Prenatal diagnosis and genetic counseling of an inherited unbalanced chromosome abnormalities in a Chinese family
by: Ying Zhang, et al.
Published: (2022-08-01)

Performance of Chromosomal Microarray Analysis for Detection of Copy Number Variations in Fetal Echogenic Bowel
by: Fan X, et al.
Published: (2021-04-01)

Clinical Utility and the Yield of Single Nucleotide Polymorphism Array in Prenatal Diagnosis of Fetal Central Nervous System Abnormalities
by: Meiying Cai, et al.
Published: (2021-05-01)

Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study
by: Huang H, et al.
Published: (2021-04-01)

Genetic counseling for a prenatal diagnosis of structural chromosomal abnormality with high-resolution analysis using a single nucleotide polymorphism microarray
by: Akiko Takashima, et al.
Published: (2016-08-01)

Prenatal Diagnosis Nomograms: A Novel Tool to Predict Fetal Chromosomal Abnormalities in High-Risk Patients
by: Zhou Y, et al.
Published: (2021-11-01)

Application of chromosomal microarray to investigate genetic causes of isolated fetal growth restriction
by: Gang An, et al.
Published: (2018-06-01)

Clinical application of single nucleotide polymorphism microarray analysis in pregnancy loss in Northwest China
by: ShuYuan Xue, et al.
Published: (2023-12-01)

Comparison of Efficiencies of Non-invasive Prenatal Testing, Karyotyping, and Chromosomal Micro-Array for Diagnosing Fetal Chromosomal Anomalies in the Second and Third Trimesters
by: Yiyang Zhu, et al.
Published: (2019-03-01)

Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency
by: Rita Cicatiello, et al.
Published: (2019-02-01)

Frequency and clinical manifestation of prenatal cytogenetic diagnosis of chromosomal polymorphisms in Northeast China
by: Li-Li Luo, et al.
Published: (2020-11-01)

Chromosomal abnormalities and copy number variations in fetal ventricular septal defects
by: Meiying Cai, et al.
Published: (2018-11-01)

Prenatal Diagnosis and Outcomes in Fetuses with Hemivertebra
by: Hang Zhou, et al.
Published: (2022-09-01)

Prenatal diagnosis of a 4.5-Mb deletion at chromosome 4q35.1q35.2: Case report and literature review
by: Gefei Xiao, et al.
Published: (2021-11-01)

Study of pregnant women with high risk of fetus abnormalities by routine cytogenetics method (karyotyping) and molecular method (FISH) by using X and Y probs and comparing the advantages and disadvantages of these methods in the northwest of Iran's patients
by: Parisa Vahidi, et al.
Published: (2021-04-01)

Chromosome Microarray Analysis and Exome Sequencing: Implementation in Prenatal Diagnosis of Fetuses with Digestive System Malformations
by: You Wang, et al.
Published: (2023-09-01)

A retrospective single-center analysis of prenatal diagnosis and follow-up of 626 chinese patients with positive non-invasive prenatal screening results
by: Xiufen Bu, et al.
Published: (2022-09-01)