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Clinical experience of noninvasive prenatal testing for rare chromosome abnormalities in singleton pregnancies

26 Sept 2022

Abstract excerpt

Objectives: The study aimed to investigate the clinical use of noninvasive prenatal testing (NIPT) for common fetal aneuploidies as a prenatal screening tool for the detection of rare chromosomal abnormalities (RCAs). Methods: Gravidas with positive NIPT results for RCAs who subsequently underwent amniocentesis for a single nucleotide polymorphism array (SNP array) were recruited. The degrees of concordance...

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Share to Genetic Syndromes and Imprinting
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

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Identifiers

PMID: 36226167
DOI: 10.3389/fgene.2022.955694

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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