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Browsing by Author Kidd, A.M.

Full Text	Issue Date	Title	Author(s)
	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