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Article

Full monosomy 21, prenatally diagnosed by fluorescent in situ hybridization.

Prenatal diagnosis - 1 Mar 1997

Joosten A M, De Vos S, Van Opstal D, Brandenburg H, Gaillard J L, Vermeij-Keers C

Abstract excerpt

We describe a case of full monosomy 21 which was prenatally diagnosed in chorionic villi by fluorescent in situ hybridization (FISH). Because of intrauterine fetal death, a curettage was performed and cytogenetic analysis of skin fibroblasts confirmed the presence of monosomy 21 in fetal cells. DNA investigations showed a paternal origin of the single chromosome 21. Inspection and autopsy of the fetus revealed...

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

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Source

Identifiers

PMID: 9110372
DOI: 10.1002/(sici)1097-0223(199703)17:3<271::aid-pd51>3.0.co;2-p

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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.

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