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Folia Biologica|June 30, 2004
Haemochromatosis-causing mutations C282Y and H63D are not risk factors for coronary artery disease in Caucasians with type 2 diabetesM Zorc, H Hruskovicová, M Globocnik Petrovic, et al.
Clinical Genetics|September 1, 1992
Prevalence of retinitis pigmentosa in SloveniaB Peterlin, N Canki-Klain, V Morela, et al.
Balkan Journal of Medical Genetics : BJMG|March 7, 2023
A Novel Likely Pathogenic Variant in the <i>RUNX1</i> Gene as the Cause of Congenital ThrombocytopeniaM Despotović, N Pereza, B Peterlin, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 1, 1997
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's syndromeA E Turco, E Bresin, S Rossetti, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|September 28, 2015
Clinical Exome Sequencing as a Novel Tool for Diagnosing Loeys-Dietz Syndrome Type 3A Blinc, A Maver, G Rudolf, et al.
Cytogenetics and Cell Genetics|January 1, 1993
An irradiation-reduced hybrid panel for fine-structure mapping of the Xq28 region in the human genomeB Peterlin, A Smahi, L Holvoet-Vermaut, et al.
Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG|December 17, 2008
Peroxisome proliferator-activated receptor gamma/Pro12Ala polymorphism and peroxisome proliferator-activated receptor gamma coactivator-1 alpha/Gly482Ser polymorphism in patients with sarcoidosisA Maver, I Medica, B Salobir, et al.
Acta Neurologica Scandinavica|November 7, 2006
Angiotensin-converting enzyme I/D gene polymorphism and risk of multiple sclerosisL Lovrecić, S Ristić, N Starcević-Cizmarević, et al.
European Journal of Neurology|December 4, 2008
Report of the Task Force on pre-graduate education in Europe of the education committee of the European Federation of Neurological Societies Composition of the task force of the education committee on pre-graduate educationJ M Lopes Lima, A Mesec, I M S Wilkinson, et al.
International Journal of Immunogenetics|July 30, 2011
CTLA-4 +49 A/G gene polymorphism in Croatian and Slovenian multiple sclerosis patientsN Starčević Cizmarević, I Gašparović, B Peterlin, et al.
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