Back to search

Article

A Retrospective Study of Noninvasive Prenatal Testing for Chromosome Aneuploidies and Sub-Chromosomal Copy Number Variations in 24359 Single Pregnancies

2020-11-13

Abstract excerpt

<title>Abstract</title> <p><bold>Background: </bold>With the development of whole-genome sequencing, small sub-chromosomal deletions and duplications could be found by non-invasive prenatal testing(NIPT). This study aimed to review the efficiency of NIPT as a screening test for aneuploidies and sub-chromosomal copy number variations (CNVs) in 24359 single pregnancies.<bold>Methods: </bold>A total of 24359 single...

Topics

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

Identifiers and source

Literature Corpus work
5ec92461-c2bc-50a2-9c21-cd39cd7b5f46
DOI
10.21203/rs.3.rs-104459/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.
A Retrospective Study of Noninvasive Prenatal Testing for Chromosome Aneuploidies and Sub-Chromosomal Copy Number Variations in 24359 Single PregnanciesDOI 10.21203/rs.3.rs-104459/v1
A retrospective study of noninvasive prenatal testing for chromosome aneuploidies and subchromosomal copy number variations in 24359 single pregnanciesSemantic proximity
Expanded Noninvasive Prenatal Testing for Chromosomal aneuploidies and Copy Number Variants in a Cohort of 16128 Single PregnanciesSemantic proximity
Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 42,910 single pregnancies with different clinical featuresSemantic proximity
Analysis of Prenatal Diagnosis Results and Pregnancy Outcome of Non-invasive Prenatal Screening High-risk FetusesSemantic proximity
Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 8141 single pregnanciesSemantic proximity
Clinical application of expanded noninvasive prenatal testing for fetal chromosome abnormalities in a cohort of 39,580 pregnanciesSemantic proximity
The Clinical Application of Non-invasive Prenatal Genetic Testing in the Screening of Fetal Chromosomal DiseasesSemantic proximity
Performance of expanded non-invasive prenatal testing for fetal aneuploidies and copy number variations: A prospective study from a single center in Jiangxi province, ChinaSemantic proximity
Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencingSemantic proximity
Non-invasive prenatal testing to detect chromosome aneuploidies in 57,204 pregnanciesSemantic proximity
Expanded non-invasive prenatal testing offers better detection of fetal copy number variations but not chromosomal aneuploidiesSemantic proximity
Clinical performance of Non-invasive prenatal testing for sex chromosomal aneuploidies in Northeast ChinaSemantic proximity
Select a neighboring publication to make it the new centre.