Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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MeSH Review:

Hyperostosis, Cortical, Congenital

Gensure, R.C. et al., Abinun, M. et al.

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High impact information on Hyperostosis, Cortical, Congenital

A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders [1].
Infantile cortical hyperostosis associated with the Wiskott-Aldrich syndrome [2].

References

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., Ala Kokko, L., Seidman, J.G., Cole, W.G., Jüppner, H. J. Clin. Invest. (2005) [Pubmed]
Infantile cortical hyperostosis associated with the Wiskott-Aldrich syndrome. Abinun, M., Mikuska, M., Filipović, B. Eur. J. Pediatr. (1988) [Pubmed]

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