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Browsing by Author Bochukova, E.G.

Full Text	Issue Date	Title	Author(s)
	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