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 microarray analysis in fetuses with congenital anomalies of the kidney and urinary tract: A prospective cohort study and meta‐analysis

16 Jan 2019

Abstract excerpt

OBJECTIVE: To evaluate the usefulness and incremental diagnostic yield of chromosomal microarray analysis (CMA) compared with standard karyotyping in fetuses with congenital anomalies of the kidney and urinary tract (CAKUT). METHODS: A prospective cohort study and systematic review of the literature were conducted. In the prospective cohort study, 123 fetuses with CAKUT, as detected by prenatal ultrasound at our...

Read the complete abstract on PubMed

Topics

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

Share to Pediatric Urology and Nephrology Studies
Share to Prenatal Screening and Diagnostics
Share to Renal and related cancers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 30650192
DOI: 10.1002/pd.5420

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Chromosomal microarray analysis in fetuses with congenital anomalies of the kidney and urinary tract: A prospective cohort study and meta‐analysisPMID 30650192Read ↗

Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in fetuses with ultrasound anomalies in the urinary systemSemantic proximity Read ↗

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

Genetic analysis and pregnancy outcomes of fetuses with kidney and urinary tract anomaliesSemantic proximity Read ↗

Chromosomal Microarray Analysis and Prenatal DiagnosisSemantic proximity Read ↗

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

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

Prenatal Chromosomal Microarray Analysis: Does Increased Resolution Equal Increased Yield?Semantic proximity Read ↗

Chromosomal Microarray Analysis in Fetuses with Growth Restriction and Normal Karyotype: A Systematic Review and Meta-AnalysisSemantic proximity Read ↗

Chromosomal Microarray versus Karyotyping for Prenatal DiagnosisSemantic proximity Read ↗

Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomaliesSemantic proximity Read ↗

Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study.Semantic proximity Read ↗

The Diagnostic Utility of Prenatal Microarray in High-Risk Pregnancies: A Single-Center Experience to Enhance Reproductive Care and Risk StratificationSemantic proximity Read ↗

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