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Browsing by Author Bauters, M.
Showing results 1 to 3 of 3
| Full Text | Issue Date | Title | Author(s) | | 2008 | Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation. | Froyen, G.; Corbett, M.; Walle, J. van de; Jarvela, I.; Lawrence, O., et al |
| 2008 | MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression. | Frints, S.G.; Lenzner, S.; Bauters, M.; Jensen, L.R.; Esch, H. van, et al |
| 2007 | Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region. | Froyen, G.; Bauters, M.; Boyle, J.; Esch, H. van; Govaerts, K., et al |
Showing results 1 to 3 of 3
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