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Browsing by Author Wilkie, A.O.

Full Text	Issue Date	Title	Author(s)
	2012	A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9	Justice, C.M.; Yagnik, G.; Kim, Y.; Peter, I.; Jabs, E.W., et al
	2009	Rare mutations of FGFR2 causing Apert syndrome : identification of the first partial gene deletion, and an Alu element insertion from a new subfamily	Bochukova, E.G.; Roscioli, T.; Hedges, D.J.; Taylor, I.B.; Johnson, D., et al
	2008	Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.	Koolen, D.A.; Sharp, A.J.; Hurst, J.A.; Firth, H.V.; Knight, S.J., et al
	2006	The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males.	Twigg, S.R.; Matsumoto, K.; Kidd, A.M.; Goriely, A.; Taylor, I.B., et al