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Article

Detection of chromosomal abnormalities in the dysmorphic fetus using fluorescence in situ hybridization: evaluation for monosomy X genotype.

Human pathology - 1 Nov 1995

Slagel D D, Bromley C M, Benda J A

Abstract excerpt

The cytogenetic abnormalities of dysmorphic fetuses who died in utero cannot be analyzed reliably by karyotyping. To overcome this obstacle, the authors applied fluorescence in situ hybridization (FISH) to formalin-fixed, paraffin-embedded tissue of two female infants and 13 female fetuses whose phenotypic features suggested possible Turner's syndrome. Previous cytogenetic evaluation of the amnionic fluid showed...

Topics

Female
Fetus
Genotype
Humans
In Situ Hybridization, Fluorescence
Infant, Newborn
Karyotyping
Monosomy
Phenotype
Placenta
Pregnancy
Sex Chromosome Aberrations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Turner Syndrome

X Chromosome

Source

Identifiers

PMID: 7590699
DOI: 10.1016/0046-8177(95)90200-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-7590699-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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Detection of chromosomal abnormalities in the dysmorphic fetus using fluorescence in situ hybridization: evaluation for monosomy X genotype.PMID 7590699Read ↗

Perinatal detection of disomy X cell line by fluorescence in situ hybridization in a pregnancy with 45,X/47,XXX at amniocentesis, cytogenetic discrepancy in various tissues and a favorable outcomeSemantic proximity Read ↗

Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridisation, (FISH)Semantic proximity Read ↗

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The rapid detection of the quantity (genotype) and cell lineage (immunophenotype) of contaminating maternal white cells in cord blood samples by fluorescence in situ hybridization combined with confocal laser scanning microscopy.Semantic proximity Read ↗

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Are all phenotypically-normal Turner syndrome fetuses mosaics?Semantic proximity Read ↗

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