Cole, William G.

A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders

Gensure, R. C., Mäkitie, O., Barclay, C., Chan, C., DePalma, S. R., Bastepe, M., Abuzahra, H., Couper, R., Mundlos, S., Sillence, D., et al. (2005) · Journal of Clinical Investigation

Connective tissue disorders researchDermatological and Skeletal Disorders

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Ehlers-Danlos Syndrome Type VII: Clinical Features and Molecular Defects*

GIUNTA, C., SUPERTI-FURGA, A., SPRANGER, S., COLE, W. G., & STEINMANN, B. (1999) · The Journal of Bone & Joint Surgery

Connective tissue disorders researchDermatological and Skeletal Disorders

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