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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
Maxwell P. Lee, Michael R. DeBaun, Kohzoh Mitsuya, Heidi L. Galonek, Sheri Brandenburg, Mitsuo Oshimura and Andrew P. FeinbergVolume:
96
Language:
english
Journal:
Proceedings of the National Academy of Sciences of the United States of America
DOI:
10.2307/47374
Date:
April, 1999
File:
PDF, 1.65 MB
english, 1999