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Browsing by Author Amiel, J.
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| 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 |
| 2006 | Loss-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 |
Showing results 1 to 2 of 2
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