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Browsing by Author Vikkula, M.
Showing results 1 to 4 of 4
| Full Text | Issue Date | Title | Author(s) | | 2006 | A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype? | Gutierrez-Roelens, I.; Roy, L. De; Ovaert, C.; Sluysmans, T.; Devriendt, K., et al |
| 1996 | Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13 | Gong, Y.; Vikkula, M.; Boon, L.; Liu, J.; Beighton, P., et al |
| 1995 | Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus | Vikkula, M.; Mariman, E.C.M.; Lui, V.C.H.; Zhidkova, N.I.; Tiller, G.E., et al |
| 1995 | Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A12 Locus | Vikkula, M.; Mariman, E.C.M.; Lui, V.C.H.; Zhidkova, N.I.; Tiller, G.E., et al |
Showing results 1 to 4 of 4
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