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A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith–Wiedemann syndrome

Nancy J. Smilinich, Colleen D. Day, Galina V. Fitzpatrick and 13 more

Proceedings of the National Academy of Sciences of the United States of America · 1999

doi:10.1073/pnas.96.14.8064 (opens in a new tab)

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Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome) · 2009
Cause and Consequences of Genetic and Epigenetic Alterations in Human Cancer · 2008

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