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Reference100 articles.
1. Van Speybroeck, L. From epigenesis to epigenetics: the case of C. H. Waddington. Ann. NY Acad. Sci. 981, 61–81 (2002).
2. Debaun, M. R. & Feinberg, A. P. in Inborn Errors of Development: The Molecular Basis of Clinical Disorders of Morphogenesis (ed. Epstein, C. J.) 758–765 (Oxford Univ. Press, Oxford, USA, 2004).
3. Niemitz, E. L. et al. Microdeletion of LIT1 in familial Beckwith–Wiedemann syndrome. Am. J. Hum. Genet. 75, 844–849 (2004).
4. Sparago, A. et al. Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith–Wiedemann syndrome. Nature Genet. 36, 958–960 (2004).
5. DeBaun, M. R. et al. Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith–Wiedemann syndrome with cancer and birth defects. Am. J. Hum. Genet. 70, 604–611 (2002).
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