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Browsing by Author Vikkula, M.

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Showing results 1 to 4 of 4
Full TextIssue DateTitleAuthor(s)
2006A 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
1996Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13Gong, Y.; Vikkula, M.; Boon, L.; Liu, J.; Beighton, P., et al
1995Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locusVikkula, M.; Mariman, E.C.M.; Lui, V.C.H.; Zhidkova, N.I.; Tiller, G.E., et al
1995Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A12 LocusVikkula, 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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