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Browsing by Author Amiel, J.

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Full TextIssue DateTitleAuthor(s)
2010IDH2 mutations in patients with D-2-hydroxyglutaric aciduria.Kranendijk, M.; Struys, E.A.; Schaftingen, E. van; Gibson, K.M.; Kanhai, W.A., et al
2006Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome.Kleefstra, T.; Brunner, H.G.; Amiel, J.; Oudakker, A.R.; Nillesen, W.M., et al
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