Lee, M. P., DeBaun, M. R., Mitsuya, K., Galonek, H. L., Brandenburg, S., Oshimura, M., & Feinberg, A. P. (1999). Loss of imprinting of a paternally expressed transcript, with antisense orientation to K(V)LQT1, occurs frequently in Beckwith–Wiedemann syndrome and is independent of insulin-like growth factor II imprinting. The National Academy of Sciences.

Lee, Maxwell P., Michael R. DeBaun, Kohzoh Mitsuya, Heidi L. Galonek, Sheri Brandenburg, Mitsuo Oshimura, and Andrew P. Feinberg. Loss of Imprinting of a Paternally Expressed Transcript, With Antisense Orientation to K(V)LQT1, Occurs Frequently in Beckwith–Wiedemann Syndrome and Is Independent of Insulin-like Growth Factor II Imprinting. The National Academy of Sciences, 1999.

Lee, Maxwell P., et al. Loss of Imprinting of a Paternally Expressed Transcript, With Antisense Orientation to K(V)LQT1, Occurs Frequently in Beckwith–Wiedemann Syndrome and Is Independent of Insulin-like Growth Factor II Imprinting. The National Academy of Sciences, 1999.