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Results: 1-13 |
Results: 13
Joint effect of G1691A factor V point mutation and factor VII Arg/Gln(353)gene polymorphism on the risk of premature coronary artery disease
Authors: Petrovic, D Zorc, M Keber, I Peterlin, B
Citation: D. Petrovic et al., Joint effect of G1691A factor V point mutation and factor VII Arg/Gln(353)gene polymorphism on the risk of premature coronary artery disease, ANN GENET, 44(1), 2001, pp. 33-36
Interaction between gene polymorphisms of renin-angiotensin system and metabolic risk factors in premature myocardial infarction
Authors: Petrovic, D Zorc, M Kanic, V Peterlin, B
Citation: D. Petrovic et al., Interaction between gene polymorphisms of renin-angiotensin system and metabolic risk factors in premature myocardial infarction, ANGIOLOGY, 52(4), 2001, pp. 247-252
Characteristics of myotonic dystrophy in Istria: Molecular genetic approach. Part II: Analysis of genetic polymorphisms
Authors: Medica, I Logar, N Peterlin, B
Citation: I. Medica et al., Characteristics of myotonic dystrophy in Istria: Molecular genetic approach. Part II: Analysis of genetic polymorphisms, COLL ANTROP, 24(2), 2000, pp. 287-294
The Str mouse as a model for Incontinentia pigmenti
Authors: Perkovic, T Duh, D Peterlin, B Gregoric, J
Citation: T. Perkovic et al., The Str mouse as a model for Incontinentia pigmenti, PFLUG ARCH, 440(5), 2000, pp. R53-R54
Angiotensin-converting enzyme gene polymorphism as a cardiovascular risk factor in children
Authors: Varda, NM Peterlin, B Bradac, SU Gregoric, A Milanez, T
Citation: Nm. Varda et al., Angiotensin-converting enzyme gene polymorphism as a cardiovascular risk factor in children, PFLUG ARCH, 439(3), 2000, pp. R34-R35
DD Genotype of the angiotensin-converting enzyme gene and stroke in Slovenian population
Authors: Peterlin, B Milanez, T Kobal, J Peterlin-Potisk, K Petrovic, D Grad, A Pogacnik, T
Citation: B. Peterlin et al., DD Genotype of the angiotensin-converting enzyme gene and stroke in Slovenian population, PFLUG ARCH, 439(3), 2000, pp. R38-R39
Deletion/insertion polymorphism in the angiotension-converting enzyme geneas a risk factor in the Slovenian patients with coronary heart disease
Authors: Peterlin, B Petrovic, D Zorc, M Keber, I
Citation: B. Peterlin et al., Deletion/insertion polymorphism in the angiotension-converting enzyme geneas a risk factor in the Slovenian patients with coronary heart disease, PFLUG ARCH, 439(3), 2000, pp. R40-R41
Effect of apolipoprotein E polymorphism and apolipoprotein A-1 gene promoter polymorphism on lipid parameters and premature coronary artery disease
Authors: Petrovic, D Zorc, M Peterlin, B
Citation: D. Petrovic et al., Effect of apolipoprotein E polymorphism and apolipoprotein A-1 gene promoter polymorphism on lipid parameters and premature coronary artery disease, FOL BIOL, 46(5), 2000, pp. 181-185
Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language
Authors: Rosser, ZH Zerjal, T Hurles, ME Adojaan, M Alavantic, D Amorim, A Amos, W Armenteros, M Arroyo, E Barbujani, G Beckman, G Beckman, L Bertranpetit, J Bosch, E Bradley, DG Brede, G Cooper, G Corte-Real, HBSM de Knijff, P Decorte, R Dubrova, YE Evgrafov, O Gilissen, A Glisic, S Golge, M Hill, EW Jeziorowska, A Kalaydjieva, L Kayser, M Kivisild, T Kravchenko, SA Krumina, A Kucinskas, V Lavinha, J Livshits, LA Malaspina, P Maria, S McElreavey, K Meitinger, TA Mikelsaar, AV Mitchell, RJ Nafa, K Nicholson, J Norby, S Pandya, A Parik, J Patsalis, PC Pereira, L Peterlin, B Pielberg, G Prata, ML Previdere, C Roewer, L Rootsi, S Rubinsztein, DC Saillard, J Santos, FR Stefanescu, G Sykes, BC Tolun, A Villems, R Tyler-Smith, C Jobling, MA
Citation: Zh. Rosser et al., Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language, AM J HU GEN, 67(6), 2000, pp. 1526-1543
Loss of heterozygosity at 11q23.1 and survival in breast cancer: Results of a large European study
Authors: Laake, K Launonen, V Niederacher, D Gudlaugsdottir, S Seitz, S Rio, P Champeme, MH Bieche, I Birnbaum, D White, G Sztan, M Sever, N Plummer, S Osorio, A Broeks, A Huusko, P Spurr, N Borg, A Cleton-Jansen, AM van't Veer, L Benitez, J Casey, G Peterlin, B Olah, E Varley, J Bignon, YJ Scherneck, S Sigurdardottir, V Lidereau, R Eyfjord, J Beckmann, MW Winqvist, R Skovlund, E Borresen-Dale, AL
Citation: K. Laake et al., Loss of heterozygosity at 11q23.1 and survival in breast cancer: Results of a large European study, GENE CHROM, 25(3), 1999, pp. 212-221
European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables
Authors: Launonen, V Laake, K Huusko, P Niederacher, D Beckmann, MW Barkardottir, RB Geirsdottir, EK Gudmundsson, J Rio, P Bignon, YJ Seitz, S Scherneck, S Bieche, I Champeme, MH Birnbaum, D White, G Varley, J Sztan, M Olah, E Osorio, A Benitez, J Spurr, N Velikonja, N Peterlin, B Borg, A Cleton-Jansen, AM Devilee, P Bloigu, R Lidereau, R Borresen-Dale, AL Winqvist, R
Citation: V. Launonen et al., European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables, BR J CANC, 80(5-6), 1999, pp. 879-882
Bilateral macular dysplasia in fragile X syndrome
Authors: Kranjc, BS Brezigar, A Peterlin, B
Citation: Bs. Kranjc et al., Bilateral macular dysplasia in fragile X syndrome, OPT VIS SCI, 75(12), 1998, pp. 856-859
Characteristics of myotonic dystrophy in Istria: Molecular genetics approach - Mutation analysis
Authors: Medica, I Logar, N Batagelj, M Peterlin, B
Citation: I. Medica et al., Characteristics of myotonic dystrophy in Istria: Molecular genetics approach - Mutation analysis, COLL ANTROP, 22(2), 1998, pp. 477-484
Risultati: 1-13 |