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

Androgenetic complete mole with trisomy 13: report of a case with microsatellite genotyping and review of the literature.

Pathology, research and practice - 15 Nov 2010

Dubé V, Chun K, Osborne R, Sherman C, Nofech-Mozes S, Ismiil N, Saad R S, Khalifa M A

Abstract excerpt

Hydatidiform moles are gestational diseases with abnormal development of the villous trophoblast and characterized by an excess of paternal to maternal genetic material. Complete moles are usually diploid and androgenetic, and are thought to develop after the fertilization of an "empty ovum" by either a haploid spermatozoon or two spermatozoa. We report a case of a complete mole in which fluorescence in situ...

Read the complete abstract on PubMed

Topics

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

Share to Chorionic Villi
Share to Chromosome Disorders

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

Share to Chromosomes, Human, Pair 13

Share to Fathers

Share to Hydatidiform Mole

Share to Trisomy

Share to Trophoblasts

Share to Uterine Neoplasms

Source

Identifiers

PMID: 20400232
DOI: 10.1016/j.prp.2010.02.013

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

Androgenetic complete mole with trisomy 13: report of a case with microsatellite genotyping and review of the literature.PMID 20400232Read ↗

Parental contribution to trisomy in heterozygous androgenetic complete moles.Semantic proximity Read ↗

Molecular genetic analysis of complete hydatidiform moles.Semantic proximity Read ↗

Androgenetic Complete Hydatidiform Moles With p57KIP2-Positive Immunostaining.Semantic proximity Read ↗

Invasive Complete Hydatidiform Moles: Analysis of a Case Series With Genotyping.Semantic proximity Read ↗

Mosaic trisomy 13: understanding origin using SNP array.Semantic proximity Read ↗

Abnormal villous morphology associated with triple trisomy of paternal origin.Semantic proximity Read ↗

Complete hydatidiform mole with retained maternal chromosomes 6 and 11.Semantic proximity Read ↗

Single-nucleotide polymorphism array and fluorescence in situ hybridization analysis to decode the cytogenetic profile of atypical partial hydatidiform moles diagnosed by short tandem repeat polymorphism analysis.Semantic proximity Read ↗

DNA Genotyping of Suspected Partial Hydatidiform Moles Detects Clinically Significant Aneuploidy.Semantic proximity Read ↗

Biparental hydatidiform moles: a maternal effect mutation affecting imprinting in the offspring.Semantic proximity Read ↗

Abnormal villous morphology mimicking a hydatidiform mole associated with paternal trisomy of chromosomes 3,7,8 and unipaternal disomy of chromosome 11.Semantic proximity Read ↗

Analysis of gestational trophoblastic disease by genotyping and chromosome in situ hybridization.Semantic proximity Read ↗

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