Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing

1 Jan 2021

Abstract excerpt

Objectives The aim of this study is to share our experience in the prenatal diagnosis of omphalocele by karyotyping, chromosomal microarray analysis (CMA) and whole exome sequencing (WES).Methods In this retrospective study, 81 cases of omphalocele were identified from 2015 to 2020. Associated anomalies and prenatal diagnosis based on karyotyping, CMA and WES were analysed.Results Fifty-eight (71.6%) of the 81...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Congenital Anomalies and Fetal Surgery
Share to Prenatal Screening and Diagnostics
Share to Tumors and Oncological Cases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34374610
DOI: 10.1080/07853890.2021.1962966

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencingPMID 34374610Read ↗

Chromosomal Abnormalities Associated With OmphaloceleSemantic proximity Read ↗

Clinical utility of trio whole exome sequencing in fetuses with ultrasound anomaliesSemantic proximity Read ↗

Clinical utility of chromosomal microarray analysis and whole exome sequencing in fetuses with oligohydramniosSemantic proximity Read ↗

Genetic Analysis of Isolated Fetal Growth RestrictionSemantic proximity Read ↗

Utility of whole exome sequencing in the evaluation of isolated fetal growth restriction in normal chromosomal microarray analysisSemantic proximity Read ↗

The evolution of prenatal Whole Exome Sequencing: from cytogenetics to precision medicineSemantic proximity Read ↗

Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imagingSemantic proximity Read ↗

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

Genetic causes of isolated and severe fetal growth restriction in normal chromosomal microarray analysisSemantic proximity Read ↗

Exome Sequencing in Fetuses with Structural MalformationsSemantic proximity Read ↗

Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital AnomaliesSemantic proximity Read ↗

Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalitiesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.