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

Analysis of the spectrum of malformations in human fetuses of the second and third trimester of pregnancy with human triploidy.

Pathologica - 1 Aug 2000

Sergi C, Schiesser M, Adam S, Otto H F

Abstract excerpt

Triploidy is constituted by an extra haploid set of chromosomes for a total of 69 chromosomes in humans. A "parent-of-origin" effect has been demonstrated by analysis of cytogenetic polymorphisms of triploidy pregnancies. Two distinct phenotypes of human triploid fetuses have been recognized according to the parental origin of the extra haploid set. The first one or triploidy of diandric type occurs when the...

Read the complete abstract on PubMed

Topics

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

Share to Face
Share to Fetal Growth Retardation
Share to Gestational Age

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

Share to Limb Deformities, Congenital

Share to Polyploidy

Share to Pregnancy Trimester, Second

Share to Pregnancy Trimester, Third

Share to Viscera

Source

Identifiers

PMID: 11029886

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

Analysis of the spectrum of malformations in human fetuses of the second and third trimester of pregnancy with human triploidy.PMID 11029886Read ↗

Prenatal sonographic features can accurately determine parental origin in triploid pregnancies.Semantic proximity Read ↗

Triploidy - variability of sonographic phenotypes.Semantic proximity Read ↗

Triploidy: Variation of Phenotype.Semantic proximity Read ↗

Triploid pregnancy-Clinical implications.Semantic proximity Read ↗

Two different phenotypes of fetuses with chromosomal triploidy: correlation with parental origin of the extra haploid set.Semantic proximity Read ↗

Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole.Semantic proximity Read ↗

Parental origin of triploidy in human fetuses: evidence for genomic imprintingSemantic proximity Read ↗

Karyotype, phenotype and parental origin in 19 cases of triploidy.Semantic proximity Read ↗

Genome‐wide abnormalities in embryos: Origins and clinical consequencesSemantic proximity Read ↗

Phenotype of triploid embryos.Semantic proximity Read ↗

"Double trouble" or an amplification of the triploidy phenotype?Semantic proximity Read ↗

Triploid pregnancies: genetic and clinical features of 158 cases.Semantic proximity Read ↗

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