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N Engl J Med In New England Journal of Medicine, Vol. 358, No. 11. (13 March 2008), pp. 1148-1159, doi:10.1056/nejmra072067 Key: citeulike:2530472
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Classic genetics alone cannot explain the diversity of phenotypes within a population. Nor does classic genetics explain how, despite their identical DNA sequences, monozygotic twins1 or cloned animals2 can have different phenotypes and different susceptibilities to a disease. The concept of epigenetics offers a partial explanation of these phenomena. First introduced by C.H. Waddington in 1939 to name ?the causal interactions between genes and their products, which bring the phenotype into being,?3 epigenetics was later defined as heritable changes in gene expression that are not due to any alteration in the DNA sequence.4 The best-known epigenetic marker is DNA methylation. . . .
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