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Article

Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues.

European journal of human genetics : EJHG - 1 Jan 2000

Wakeling E L, Abu-Amero S N, Stanier P, Preece M A, Moore G E

Abstract excerpt

Maternal uniparental disomy of chromosome 7 (mUPD7) has been reported in around 10% of cases of Silver-Russell syndrome (SRS). This suggests that at least one gene on chromosome 7 is imprinted and involved in the pathogenesis of this condition. One candidate is epidermal growth factor receptor (EGFR) which maps to chromosome 7p12, a region homologous to an imprinted region on mouse chromosome 11. Using a...

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PMID: 9781061
DOI: 10.1038/sj.ejhg.5200179

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EGFR

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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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Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues.PMID 9781061Read ↗

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The genetic aetiology of Silver-Russell syndrome.Semantic proximity Read ↗

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No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients.Semantic proximity Read ↗

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