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Article

Mosaic triple trisomy in amniocytes from a phenotypically and karyotypically normal fetus.

Prenatal diagnosis - 1 Mar 1994

Mascarello J T, Jones M C, Catanzarite V A, Brown K H

Abstract excerpt

We report the detection of a mosaic triple trisomy, 46,XY/49,XY,+13,+20,+21, in two amniotic fluid specimens obtained from a pregnancy that yielded a normal infant. Traditional cytogenetic methods failed to detect the abnormal cell lineage in fetal blood, foreskin, amnion, umbilical cord, and three different biopsies of the chorion. In addition, fluorescence in situ hybridization study of cells from a buccal...

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Identifiers

PMID: 8052562
DOI: 10.1002/pd.1970140303

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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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