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Results: 1-8 |
Results: 8
The heart of the matter - New insights into the genetics of cardiomyopathy
Authors: Wadelius, C
Citation: C. Wadelius, The heart of the matter - New insights into the genetics of cardiomyopathy, SC CARDIOVA, 34(6), 2000, pp. 547-547
Prostate cancer associated with CYP17 genotype
Authors: Wadelius, M Andersson, SO Johansson, JE Wadelius, C Rane, A
Citation: M. Wadelius et al., Prostate cancer associated with CYP17 genotype, PHARMACOGEN, 9(5), 1999, pp. 635-639
Polymorphisms in NAT2, CYP2D6, CYP2C19 and GSTP1 and their association with prostate cancer
Authors: Wadelius, M Autrup, JL Stubbins, MJ Andersson, SO Johansson, JE Wadelius, C Wolf, CR Autrup, H Rane, A
Citation: M. Wadelius et al., Polymorphisms in NAT2, CYP2D6, CYP2C19 and GSTP1 and their association with prostate cancer, PHARMACOGEN, 9(3), 1999, pp. 333-340
Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies
Authors: Allikmets, R Seddon, JM Bernstein, PS Hutchinson, A Atkinson, A Sharma, S Gerrard, B Li, W Metzker, ML Wadelius, C Caskey, CT Dean, M Petrukhin, K
Citation: R. Allikmets et al., Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies, HUM GENET, 104(6), 1999, pp. 449-453
The mutation spectrum of the bestrophin protein - functional implications
Authors: Bakall, B Marknell, T Ingvast, S Koisti, MJ Sandgren, O Li, W Bergen, AAB Andreasson, S Rosenberg, T Petrukhin, K Wadelius, C
Citation: B. Bakall et al., The mutation spectrum of the bestrophin protein - functional implications, HUM GENET, 104(5), 1999, pp. 383-389
Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n)
Authors: Spath, PJ Sjoholm, AG Fredrikson, GN Misiano, G Scherz, R Schaad, UB Uhring-Lambert, B Hauptmann, G Westberg, J Uhlen, M Wadelius, C Truedsson, L
Citation: Pj. Spath et al., Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n), CLIN EXP IM, 118(2), 1999, pp. 278-284
Further evidence of genetic homogeneity in Sjogren-Larsson syndrome
Authors: Pigg, M Annton-Lamprecht, I Braun-Quentin, C Gustavson, KH Wadelius, C
Citation: M. Pigg et al., Further evidence of genetic homogeneity in Sjogren-Larsson syndrome, ACT DER-VEN, 79(1), 1999, pp. 41-43
Centrotemporal spikes in families with rolandic epilepsy - Linkage to chromosome 15q14
Authors: Neubauer, BA Fiedler, B Himmelein, B Kampfer, F Lassker, U Schwabe, G Spanier, I Tams, D Bretscher, C Moldenhauer, K Kurlemann, G Weise, S Tedroff, K Eeg-Olofsson, O Wadelius, C Stephani, U
Citation: Ba. Neubauer et al., Centrotemporal spikes in families with rolandic epilepsy - Linkage to chromosome 15q14, NEUROLOGY, 51(6), 1998, pp. 1608-1612
Risultati: 1-8 |