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Article

Del(3) (p25.3) without phenotypic effect.

Journal of medical genetics - 1 Dec 1995

Knight L A, Yong M H, Tan M, Ng I S

Abstract excerpt

A terminal deletion of chromosome 3 at p25.3 was observed during prenatal diagnosis. A similar deletion is also present in the phenotypically normal mother. The deletion was confirmed by FISH. The breakpoint is distal to the region responsible for the 3p- syndrome. A normal baby girl was born with no apparent phenotypic abnormalities.

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Source

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Identifiers

PMID: 8825934
DOI: 10.1136/jmg.32.12.994
PMCID: PMC1051787

Provenance

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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