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

Utility of fetal karyotype in the evaluation of phenotypically abnormal stillbirths.

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society - 1 Jan 2000

Pinar Halit, Carpenter Marshall, Martin Benjamin J, Tantravahi Umadevi

Abstract excerpt

The objectives of this study are to test the hypothesis that stillbirths without aneuploidy-associated phenotypes have a low incidence of karyotypic abnormalities, similar among those with and without other anatomic defects. We employed a uniform postmortem protocol to examine fetuses and placentas in 962 consecutive stillbirths measuring > or =20 weeks in clinically determined gestational age submitted to the...

Read the complete abstract on PubMed

Topics

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

Share to Aneuploidy
Share to Chromosome Aberrations

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Chromosome Banding

Share to Fetal Diseases

Share to Gestational Age

Share to Karyotyping

Share to Stillbirth

Source

Identifiers

PMID: 19021454
DOI: 10.2350/07-07-0307.1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Utility of fetal karyotype in the evaluation of phenotypically abnormal stillbirths.PMID 19021454Read ↗

Karyotype versus Microarray Testing for Genetic Abnormalities after StillbirthSemantic proximity Read ↗

Cytogenetic Analysis After Evaluation of 750 Fetal DeathsSemantic proximity Read ↗

Stillbirth Risk Among Fetuses With Ultrasound-Detected Isolated Congenital AnomaliesSemantic proximity Read ↗

The role of DNA microarrays in the evaluation of fetal deathSemantic proximity Read ↗

Wisconsin Stillbirth Service Program: II. Analysis of diagnoses and diagnostic categories in the first 1,000 referralsSemantic proximity Read ↗

Fetal ultrasound abnormalities: Correlation with fetal karyotype, autopsy findings, and postnatal outcome—five‐year prospective studySemantic proximity Read ↗

Differentiation of genetic abnormalities in early pregnancy lossSemantic proximity Read ↗

Genetics of StillbirthSemantic proximity Read ↗

Stillbirth and neonatal mortality in pregnancies complicated by major congenital anomalies: Findings from a large European cohortSemantic proximity Read ↗

Genetics and Stillbirth.Semantic proximity Read ↗

RETIRED: Fetal and Perinatal Autopsy in Prenatally Diagnosed Fetal Abnormalities With Normal KaryotypeSemantic proximity Read ↗

Genomic autopsy to identify underlying causes of pregnancy loss and perinatal deathSemantic proximity Read ↗

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