Back to search

Article

Enhanced Detection of Genetic Abnormalities in High-Risk Pregnancies Using CNV-Seq Compared to Karyotyping

2026-04-07

Abstract excerpt

<title>Abstract</title> <p>Genetic abnormalities in high-risk pregnancies present substantial threats to both maternal and fetal well-being, frequently resulting in poor outcomes and imposing significant burdens on healthcare resources. This study aimed to evaluate the efficacy of copy number variation sequencing (CNV-seq) compared to karyotyping in identifying genetic abnormalities among high-risk pregnant women...

Topics

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

Identifiers and source

Literature Corpus work
cf2b5bbc-de68-5067-97eb-50327877b503
DOI
10.21203/rs.3.rs-8996177/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Enhanced Detection of Genetic Abnormalities in High-Risk Pregnancies Using CNV-Seq Compared to KaryotypingDOI 10.21203/rs.3.rs-8996177/v1
Select a neighboring publication to make it the new centre.