G. Ashworth

Hemifacial hypoplasia and hypomelanosis of Ito.

M. Poole, S. Slaney, S. Tan, 1995, Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery.

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

W. Reardon, D. David, R. Winter, 1995, Nature Genetics.

Vertical Orbital Dystopia

M. D. Poole, M. Briggs, G. Ashworth, 1996, Plastic and reconstructive surgery.

Craniofrontonasal dysplasia.

M. Poole, D. Orr, S. Slaney, 1997, British Journal of Plastic Surgery.

A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.

L. Kearney, P. Njølstad, S. Twigg, 1998, American journal of human genetics.

Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosis

M. Muenke, C. Francomano, I. Glass, 1997, The Lancet.