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Browsing by Author Kress, W.
Showing results 1 to 4 of 4
| Full Text | Issue Date | Title | Author(s) | | 2011 | Myotonic dystrophy type 2 (DM2) and related disorders report of the 180th ENMC workshop including guidelines on diagnostics and management 3-5 December 2010, Naarden, The Netherlands. | Udd, B.; Meola, G.; Krahe, R.; Wansink, D.G.; Bassez, G., et al |
| 2008 | Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome. | Schulz, A.L.; Albrecht, B.; Arici, C.; Burgt, I. van der; Buske, A., et al |
| 2007 | Encephalomyopathy and optic atrophy with tall stature and mitochondrial dysfunction: a new syndrome. | Morava, E.; Bongers, E.M.H.F.; Kress, W.; Sie, L.T.L.; Rodenburg, R.J.T., et al |
| 2004 | Partial craniosynostosis in a patient with deletion 22q11. | Karteszi, J.; Kress, W.; Szasz, M.; Czako, M.; Melegh, B., et al |
Showing results 1 to 4 of 4
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