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Browsing by Author Teszas, A.
Showing results 1 to 4 of 4
| Full Text | Issue Date | Title | Author(s) | | 2006 | Presenile cataract: consider cholestanol. | Teszas, A.; Pfund, Z.; Morava, E.; Kosztolanyi, G.Y.; Sistermans, E.A., et al |
| 2006 | Females with PDHA1 gene mutations: a diagnostic challenge. | Willemsen, M.A.A.P.; Rodenburg, R.J.T.; Teszas, A.; Heuvel, L.P.W.J. van den; Kosztolanyi, G.Y., et al |
| 2006 | Expanding the clinical spectrum of MYCN-related Feingold syndrome. | Teszas, A.; Meijer, R.; Scheffer, H.; Gyuris, P.; Kosztolanyi, G.Y., et al |
| 2004 | Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patients. | Karteszi, J.; Hollody, K.; Bene, J.; Morava, E.; Hadzsiev, K., et al |
Showing results 1 to 4 of 4
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