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 Associated With Omphalocele

1 Mar 2007

Abstract excerpt

Fetuses with omphalocele have an increased risk for chromosomal abnormalities. The risk varies with maternal age, gestational age at diagnosis, association with umbilical cord cysts, complexity of associated anomalies, and the contents of omphalocele. There is considerable evidence that genetics contributes to the etiology of omphalocele. This article provides an overview of chromosomal abnormalities associated...

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 Congenital Diaphragmatic Hernia Studies
Share to Urological Disorders and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 17389182
DOI: 10.1016/s1028-4559(08)60099-6

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

Chromosomal Abnormalities Associated With OmphalocelePMID 17389182Read ↗

Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencingSemantic proximity Read ↗

Syndromes and Disorders Associated with Omphalocele (III): Single Gene Disorders, Neural Tube Defects, Diaphragmatic Defects and OthersSemantic proximity Read ↗

Anatomic parameters of omphaloceles and their association with anatomic, genetic, or syndromic malformations: a retrospective studySemantic proximity Read ↗

Syndromes and disorders associated with omphalocele (I): Beckwith-Wiedemann syndrome.Semantic proximity Read ↗

Prevalence, Correlates, and Outcomes of Omphalocele in the United States, 1995–2005Semantic proximity Read ↗

Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcome.Semantic proximity Read ↗

Chromosomal abnormalities in fetuses with open neural tube defects: prenatal identification with ultrasoundSemantic proximity Read ↗

Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele.Semantic proximity Read ↗

Holoprosencephaly: recommendations for diagnosis and management.Semantic proximity Read ↗

Chromosomal Abnormalities Associated with Neural Tube Defects (II): Partial AneuploidySemantic proximity Read ↗

Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformationsSemantic proximity Read ↗

Omphalocele and gastroschisis: An 18-year review studySemantic proximity Read ↗

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