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Article

Mild phenotypic manifestation of a 7p15.3p21.2 deletion.

Journal of medical genetics - 1 Jul 1993

Wang C, Maynard S, Glover T W, Biesecker L G

Abstract excerpt

A 28 month old girl with dysmorphic features was found to have an interstitial deletion of the short arm of chromosome 7p15.3-7p21.2. The patient had ptosis, dacryostenosis, pectus excavatum, short hands, and her development was normal or mildly delayed. Craniosynostosis and growth retardation, which were present in two other patients with similar deletions, were not present. Because of the mild manifestations,...

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Identifiers

PMID: 8411039
DOI: 10.1136/jmg.30.7.610
PMCID: PMC1016466

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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