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Article

Insulin-like growth factor I gene deletion causing intrauterine growth retardation and severe short stature.

Acta paediatrica (Oslo, Norway : 1992). Supplement - 1 Nov 1997

Woods K A, Camacho-Hübner C, Barter D, Clark A J, Savage M O

Abstract excerpt

The first human case of a homozygous molecular defect in the gene encoding insulin-like growth factor I (IGF-I) is described. The patient was a 15-year-old boy from a consanguineous pedigree who presented with severe intrauterine growth failure, sensorineural deafness and mild mental retardation....

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Identifiers

PMID: 9401537
DOI: 10.1111/j.1651-2227.1997.tb18367.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-9401537-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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