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Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
Lee, M. P., DeBaun, M. R., Mitsuya, K., Galonek, H. L., Brandenburg, S., Oshimura, M., Feinberg, A. P.Volume:
96
Language:
english
Journal:
Proceedings of the National Academy of Sciences
DOI:
10.1073/pnas.96.9.5203
Date:
April, 1999
File:
PDF, 247 KB
english, 1999