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Oldenburg, Johannes; Fregin, A.; Rost S.; Wolz, W.; Krebsova, A.; Müller, C.R.: Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K-dependent clotting factors (FMFD) to the centromeric region of chromosome 16. In: Blood, 100(9), 2002, S. 3229-3232

Oldenburg, Johannes; Rost, S.; Fregin, A.; Ivaskevicius, V.; Conzelmann, E.; Hörtnagel, K.; Pelz, H.-J.; Lappegard, K.; Seifried, E.; Scharrer, I.; Tuddenham, E.G.D.; Müller, CR.; Strom, T.M.: Mutations in the VKORC1 gene cause warfarin resistance and multiple coagulation factor deficiency type 2. In: Nature, 427(6974), 2004, S. 537-541

Oldenburg, Johannes; El-Maarri, O.; Herbiniaux, U.; Graw, J.; Schroder, J.; Terzic, A.; Watzka, M.; Brackmann, H.H.; Schramm, W.; Hanfland, P.; Schwaab, R.; Muller, C.R.: Analysis of mRNA in hemophilia A patients with undetectable mutations reveals normal splicing in the factor VIII gene. In: Journal of Thrombosis and Haemostasis, 3(2), 2005, S. 332-339

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