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Article

Molecular genetics of Wiedemann-Beckwith syndrome

2 Oct 1998

Abstract excerpt

Wiedemann-Beckwith syndrome (WBS) is a heterogeneous overgrowth syndrome associated with malformations and an elevated risk of developing embryonal tumors. WBS is a multigenic disorder caused by dysregulation of imprinted growth regulatory genes within the 11p15 region. Elucidation of the genetic cause of WBS will provide important insights into the molecular and epigenetic changes associated with loss of normal...

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Identifiers

PMID: 9781904
DOI: 10.1002/(sici)1096-8628(19981002)79:4<253::aid-ajmg5>3.0.co;2-n

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Source receipt: pubmed, retrieved 7 Sept 2026.

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