Kaija Kuurila-Svahn

Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans

F. Glorieux, P. Byers, J. Troendle, 2007, Human mutation.

Skull base abnormalities in osteogenesis imperfecta: a cephalometric evaluation of 54 patients and 108 control volunteers.

I. Kaitila, S. Pynnönen, O. Kovero, 2006, Journal of neurosurgery.