W Bickmore

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

W. Reik, W. Bickmore, Y. Le Bouc, 1995, Human molecular genetics.

Human diseases with underlying defects in chromatin structure and modification.

W. Bickmore, B. Hendrich, W Bickmore, 2001, Human molecular genetics.