Tom Stiff

发表

Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome

Penny A Jeggo, Claudia Kerzendorfer, P. Jeggo, 2011, Nature Genetics.

Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling

William C Earnshaw, Bertrand Vernay, Penny A Jeggo, 2008, Nature Genetics.

ATR promotes cilia signalling: links to developmental impacts

Penny A. Jeggo, P. Jeggo, M. Philipp, 2016, Human molecular genetics.