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Article

Mosaicism for 47,XXY or 47,XXY/46,XY at amniocentesis in a pregnancy with a favorable outcome and no prominent perinatal decrease of the 47,XXY cell line

1 Jul 2024

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 39004494
DOI: 10.1016/j.tjog.2024.05.016

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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Click a neighbor to travelStep 1 · 12 closest

Mosaicism for 47,XXY or 47,XXY/46,XY at amniocentesis in a pregnancy with a favorable outcome and no prominent perinatal decrease of the 47,XXY cell linePMID 39004494Read ↗

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 fetal outcome and postnatal decrease of the 45,X cell lineSemantic proximity Read ↗

45,X/46,XX at amniocentesis associated with a favorable 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 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 ↗

Mosaic 46,XX,der(9)t(9;13)(p24;q12)/46,XX at amniocentesis can be a culture artefact and associated with a favorable fetal outcomeSemantic proximity Read ↗

Positive non-invasive prenatal testing for Turner syndrome and low-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy associated with a favorable fetal outcome and a normal 46,XX karyotype at birthSemantic proximity Read ↗

45,X/46,XX mosaicism in patients with idiopathic premature ovarian failureSemantic 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 ↗

46,XY/47,XY,+ 17p+ mosaicism in amniocytes associated with fetal abnormalities despite normal fetal blood karyotypeSemantic 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 ↗

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

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