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LIT1 and H19 methylation defects in isolated hemihyperplasia
Rick A Martin1, Dorothy K Grange, Babara Zehnbauer
1Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA. martin_r@kids.wustl.edu
Abstract:
We performed LIT1 and H19 methylation studies on 27 children with isolated hemihyperplasia (IH). Eight children (29.6%) had a defect in methylation of one or both of these alleles, supporting our hypothesis that these epigenetic changes can result in a phenotype distinct from typical Beckwith-Wiedemann syndrome.
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