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

Genetic causes of isolated and severe fetal growth restriction in normal chromosomal microarray analysis

10 Dec 2022

Abstract excerpt

OBJECTIVE: To investigate the genetic burden in fetuses with isolated and severe fetal growth restriction (FGR) using Trio whole-exome sequencing (WES) with a normal chromosomal microarray. METHOD: This retrospective study analyzed WES results of singleton fetuses with isolated and severe FGR, whose estimated fetal weight (EFW) was less than the third percentile by Hadlock formula, in a tertiary center between...

Read the complete abstract on PubMed

Topics

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

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 36495297
DOI: 10.1002/ijgo.14620

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic causes of isolated and severe fetal growth restriction in normal chromosomal microarray analysisPMID 36495297Read ↗

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 ↗

Detection of chromosomal and gene abnormality with karyotyping, chromosomal microarray analysis and trio-based whole exome sequencing in pregnancies with fetal growth restriction: implications for precise prenatal diagnosisSemantic proximity Read ↗

Genetics Etiologies Associated with Fetal Growth RestrictionSemantic proximity Read ↗

Genetic syndromes associated with isolated fetal growth restrictionSemantic proximity Read ↗

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

Contribution of uniparental disomy to fetal growth restriction: a whole-exome sequencing series in a prenatal settingSemantic proximity Read ↗

Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalisSemantic proximity Read ↗

Prenatal Whole-exome Sequencing in a Russian Clinical Cohort: Diagnostic Yield, Indications, and Spectrum of Molecular FindingsSemantic proximity Read ↗

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

Idiopathic polyhydramnios and postnatal outcomes of children: The role of exome sequencingSemantic proximity Read ↗

Comprehensive genome sequencing analysis as a promising option in the prenatal diagnosis of fetal structural anomalies: a prospective studySemantic proximity Read ↗

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