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Article

Constitutional H19 hypermethylation in a patient with isolated cardiac tumor.

American journal of medical genetics. Part A - 15 Aug 2008

Descartes Maria, Romp Robb, Franklin Judy, Biggio Joseph R, Zehnbauer Barbara

Abstract excerpt

Beckwith-Wiedemann syndrome (BWS) is clinically and molecularly very heterogenous. Molecular findings characteristic of BWS have been reported in individuals with no or few associated features. We report on a child with isolated cardiac tumor and a constitutional H19 hypermethylation with none of the features of BWS.

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Share to Beckwith-Wiedemann Syndrome
Share to Chromosomes, Human, Pair 11
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18627058
DOI: 10.1002/ajmg.a.32421

Provenance

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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