Article

Combined Application of Chromosome Karyotype and Microarray Analysis in Fetus With Increased Nuchal Translucency

2021-05-24

Abstract excerpt

<h4>Objective: </h4> ： To examine the risk of chromosomal abnormalities when the thickness of the nuchal translucency( NT ) is 2.5-2.9mm, to evaluate the cutoff value of NT for prenatal diagnosis, to explore the value of combined application of chromosome karyotype and microarray analysis, and to explore the relationship between NT ≥ 5.0mm and fetal prognosis. <h4>Methods: </h4>： A total of 366 pregnant women who...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: d45f55bc-b683-5500-8670-ede4a94efed6
DOI: 10.21203/rs.3.rs-524636/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Combined Application of Chromosome Karyotype and Microarray Analysis in Fetus With Increased Nuchal TranslucencyDOI 10.21203/rs.3.rs-524636/v1Read

Associations between genomic aberrations, increased nuchal translucency, and pregnancy outcomes: a comprehensive analysis of 2,272 singleton pregnancies in women under 35Semantic proximity Read

The Role of Thickened Nuchal Translucency on Copy Number Variations and Pregnancy Outcomes in Northeast Coast of Fujian Province, China: A Comparison Between Traditional Karyotyping and Single Nucleotide Polymorphism Array AnalysisSemantic proximity Read

Ultrasonographic Fetal Nuchal Translucency Measurements and Cytogenetic OutcomesSemantic proximity Read

Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotypeSemantic proximity Read

Increased nuchal translucency thickness and normal chromosomal microarray: Danish nationwide cohort studySemantic proximity Read

Outcomes associated with fetal nuchal translucency between 3.0 and 3.4 mm in the first trimesterSemantic proximity Read

A retrospective study for diagnostic value of chromosomal microarray analysis in fetuses with high-risk prenatal indicationsSemantic proximity Read

Genetic correlation between fetal nuchal translucency thickening and cystic hygroma and exploration of pregnancy outcomeSemantic proximity Read

Molecular genetic and pregnancy outcomes of fetuses with increased Nuchal Translucency.Semantic proximity Read

Diagnostic Value of Karyotyping, CMA/CNV-Seq, and WES in Fetuses with Thickened Nuchal Translucency: Perinatal and Two-Year Follow-Up OutcomesSemantic proximity Read

Chromosomal Microarray Analysis and Karyotype Analysis for Prenatal Diagnosis of Fetuses With Abnormal Ultrasound Soft MarkersSemantic proximity Read

Genetic Examination for Fetuses with Increased Fetal Nuchal Translucency by Genomic TechnologySemantic proximity Read