Author:
Reardon William,Winter Robin M.,Rutland Paul,Pulleyn Louise J.,Jones Barry M.,Malcolm Sue
Publisher
Springer Science and Business Media LLC
Reference37 articles.
1. Cohen, M.M.Jr, Craniosynostosis: diagnosis, evaluation and management. (Raven Press, New York, 1986).
2. Winter, R.M. & Baraitser, M. The London Dysmorphology Database. (Oxford University Press, Oxford, 1994).
3. Warman, M.L., Mulliken, J.B., Hayward, P.G. & Muller, U. Newly recognised autosomal dominant craniosynostotic syndrome. Am. J. med. Genet. 46, 444–449 (1993).
4. Muller, U., Warman, M.L., Mulliken, J.B. & Weber, J. Assignment of a gene locus Involved in craniosynostosis to chromosome 5qter. Hum. molec. Genet. 2, 119–122 (1992).
5. Jabs, E.W. et al. Mutation in the Homeodomain of the Human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell 75, 443–450 (1993).
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