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- W2014155499 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. © 2005 Wiley-Liss, Inc." @default.
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- W2014155499 date "2005-01-01" @default.
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- W2014155499 title "LIT1 andH19 methylation defects in isolated hemihyperplasia" @default.
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- W2014155499 doi "https://doi.org/10.1002/ajmg.a.30578" @default.
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