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

Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies

12 Apr 2019

Abstract excerpt

OBJECTIVES: To evaluate the incidence and types of chromosomal abnormalities detected in twins with structural anomalies and compare their distribution according to chorionicity and amnionicity and by structural-anomaly type. The added value of chromosomal microarray analysis (CMA) over conventional karyotyping in twins was also estimated. METHODS: This was a single-center, retrospective analysis of 534 twin...

Read the complete abstract on PubMed

Topics

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

Share to Assisted Reproductive Technology and Twin Pregnancy
Share to Congenital Anomalies and Fetal Surgery
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 30977228
DOI: 10.1002/uog.20287

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

Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomaliesPMID 30977228Read ↗

Prenatal Diagnosis Using Chromosomal Microarray Analysis in High-Risk PregnanciesSemantic proximity Read ↗

Diagnostic performance of chromosomal microarray and whole exome sequencing in fetal structural anomalies: a single-center retrospective studySemantic proximity Read ↗

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

Chromosomal Microarray versus Karyotyping for Prenatal DiagnosisSemantic proximity Read ↗

Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive casesSemantic proximity Read ↗

Genetic evaluation for twin pregnancies using karyotyping and single nucleotide polymorphism array analysis.Semantic proximity Read ↗

Chromosomal Abnormalities Detected by Chromosomal Microarray Analysis and Karyotype in Fetuses with Ultrasound AbnormalitiesSemantic proximity Read ↗

Combined use of karyotyping and copy number variation sequencing technology in prenatal diagnosisSemantic proximity Read ↗

Detection of submicroscopic chromosomal aberrations by chromosomal microarray analysis for the prenatal diagnosis of central nervous system abnormalitiesSemantic proximity Read ↗

Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic AnomaliesSemantic proximity Read ↗

Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective studySemantic proximity Read ↗

Chromosomal Microarray Analysis and Prenatal DiagnosisSemantic proximity Read ↗

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