Lee M.P. et al. 1999


Lee M.P., DeBaun M.R., Mitsuya K., Galonek H.L., Brandenburg S., Oshimura M., and Feinberg A.P., 1999. 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. Proc. Natl. Acad. Sci. 96: 5203-5208.

Смотрите также:

  • Эпигенетика и BWS (синдром Беквита-Видемана)