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

Prenatal diagnosis of 46,XY/46,XX mosaicism: a case report.

American journal of medical genetics - 7 May 1999

Yaron Y, Feldman B, Kramer R L, Kasperski S B, Vo T, Feldman G L, Johnson M P, Evans M I, Ebrahim S A

Abstract excerpt

We report on the prenatal diagnosis of a fetus with 46,XY and 46,XX cell lines with a normal male phenotype. Cytogenetic and molecular studies ruled out the possibility of maternal cell contamination and showed that all the X chromosomes present in both fetal cell lines were derived from a single maternal X chromosome. This suggests 46,XY/46,XX mosaicism.

Read the complete abstract on PubMed

Topics

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

Share to Apolipoproteins B
Share to Chimera
Share to Fetus

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Meiosis

Share to Mitosis

Share to Mosaicism

Share to Prenatal Diagnosis

Share to Sex Chromosomes

Source

Identifiers

PMID: 10213039

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prenatal diagnosis of 46,XY/46,XX mosaicism: a case report.PMID 10213039Read ↗

High-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a fetus with a favorable fetal outcome and the karyotype of 46,XX in the neonatal peripheral blood at age 4½ monthsSemantic proximity Read ↗

High-level mosaicism for 45,X in 45,X/46,X,+mar at amniocentesis in a pregnancy associated with positive non-invasive prenatal testing for Turner syndrome, normal male external genitalia and positive SRY in the fetus, a favorable fetal outcome, postnatal decrease of the 45,X cell line and cytogenetic discrepancy in various tissuesSemantic proximity Read ↗

Prenatal diagnosis of 45,X and 45,X mosaicism: the need for thorough cytogenetic and clinical evaluationsSemantic proximity Read ↗

High-level mosaicism for 45,X in 45,X/46, XY at amniocentesis in a pregnancy with a favorable fetal outcome and cytogenetic discrepancy in various tissuesSemantic proximity Read ↗

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

Rare XXY/XX mosaicism in a phenotypic male with Klinefelter syndrome: case report.Semantic proximity Read ↗

Turner phenotype in a girl with a 45,X/46,XX/47,XX,+18 mosaicism.Semantic proximity Read ↗

High-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy with a favorable fetal outcome and postnatal decrease of the 45,X cell lineSemantic proximity Read ↗

Perinatal cytogenetic discrepancy in a pregnancy with mosaic 45,X/46, XY at amniocentesis and a favorable outcomeSemantic proximity Read ↗

Low-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy with a favorable fetal outcome and postnatal decrease of the 45,X cell lineSemantic proximity Read ↗

High-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell lineSemantic proximity Read ↗

Prenatal diagnosis of 46, XX male fetusSemantic proximity Read ↗

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