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Browsing by Author Grange, D.K.

Full Text	Issue Date	Title	Author(s)
	2010	IDH2 mutations in patients with D-2-hydroxyglutaric aciduria.	Kranendijk, M.; Struys, E.A.; Schaftingen, E. van; Gibson, K.M.; Kanhai, W.A., et al
	2005	Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.	Johnston, J.J.; Olivos-Glander, I.; Killoran, C.; Elson, E.; Turner, J.T., et al