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

A case of 46,XX/46,XX chimerism in a phenotypically normal woman.

International journal of legal medicine - 1 Nov 2020

Cho Sohee, Lee Hwan Young, Kim Moon-Young, Lyoo Sung-Hee, Lee Soong Deok

Abstract excerpt

Chimerism is the presence of two genetically different cell lines within a single organism, which is rarely observed in humans. Usually, chimerism in the human body is revealed by the finding of an abnormal phenotype during a medical examination or is unexpectedly detected in routine genetic analysis. However, the incidence or underlying mechanism of chimerism remains unclear due to the lack of information on...

Read the complete abstract on PubMed

Topics

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

Share to Chimerism
Share to Chromosomes, Human, X
Share to DNA

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fertilization

Share to Gene Frequency

Share to Genetic Loci

Share to Karyotype

Share to Microsatellite Repeats

Source

Identifiers

PMID: 32361859
DOI: 10.1007/s00414-020-02296-y

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A case of 46,XX/46,XX chimerism in a phenotypically normal woman.PMID 32361859Read ↗

A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia.Semantic proximity Read ↗

High-level 46XX/46XY chimerism without clinical effect in a healthy multiparous female.Semantic proximity Read ↗

A prenatal case misunderstood as specimen confusion: 46,XY/46,XY chimerism.Semantic proximity Read ↗

A dispermic chimera was identified in a healthy man with mixed field agglutination reaction in ABO blood grouping and mosaic 46, XY/46, XX karyotype.Semantic proximity Read ↗

Chimerism in the immunohematology laboratory in the molecular biology era.Semantic proximity Read ↗

Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimeraSemantic proximity Read ↗

Identification of the mechanism underlying a human chimera by SNP array analysis.Semantic proximity Read ↗

Chimerism resulting from parthenogenetic activation and dispermic fertilizationSemantic proximity Read ↗

Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case report.Semantic proximity Read ↗

Chimera and other fertilization errorsSemantic proximity Read ↗

Dispermic chimerism with two abnormal cell lines, 47,XY, +21 and 47,XX, +12Semantic proximity Read ↗

A dispermic chimerism detected in a Taiwanese potential unrelated hematopoietic stem cell donor.Semantic proximity Read ↗

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