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Article

Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor

27 Jul 2005

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Share to Epigenetics and DNA Methylation
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16049499
DOI: 10.1038/ng0805-785

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Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumorPMID 16049499Read ↗

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Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.Semantic proximity Read ↗

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.Semantic proximity Read ↗

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Beckwith-Wiedemann Syndrome: Historical, Clinicopathological, and Etiopathogenetic PerspectivesSemantic proximity Read ↗

Paternally Inherited Submicroscopic Duplication at 11p15.5 Implicates Insulin-like Growth Factor II in Overgrowth and Wilms' TumorigenesisSemantic proximity Read ↗

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