Poole, R. L., Leith, D. J., Docherty, L. E., Shmela, M. E., Gicquel, C., Splitt, M., . . . Mackay, D. J. G. (2012). Beckwith–Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1. Nature Publishing Group.

Poole, Rebecca L., Donald J. Leith, Louise E. Docherty, Mansur E. Shmela, Christine Gicquel, Miranda Splitt, I Karen Temple, and Deborah J G. Mackay. Beckwith–Wiedemann Syndrome Caused By Maternally Inherited Mutation of an OCT-binding Motif in the IGF2/H19-imprinting Control Region, ICR1. Nature Publishing Group, 2012.

Poole, Rebecca L., et al. Beckwith–Wiedemann Syndrome Caused By Maternally Inherited Mutation of an OCT-binding Motif in the IGF2/H19-imprinting Control Region, ICR1. Nature Publishing Group, 2012.