Претрага
Резултати
Cardiac disorders in BMD patients with distal gene deletions [2002]
Novaković, I.8 year experience in molecular prenatal diagnostics of cystic fibrosis in Yugoslavia - problems and future trends [1998]
Radojković, DragicaThalassemia syndromes in Serbia:the importance of genetic (re)analysis [2025]
Ugrin, Milena M; Komazec, Jovana; Klaassen, Kristel M
Pavlovic, Sonja T; Stojiljkovic, Maja M;
Analysis of association of MMP-2 gene promoter haplotype with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis
[2020]
Grk, Milka B. Chromosomal microarray analysis in children with syndromic short stature
[2024]
Maksimović, Nela Internal Skeletal Dysplasia Registry within the electronic database of Department of Clinical Genetics University Children's Hospital in Belgrade - basis for a personalised medicine in the future [2023]
Mijovic, Marija; Cuturilo, Goran; Ruml-Stojanovic, Jelena; Miletic, Aleksandra; Bosankic, Brankica; Petrovic, HristinaGlycogen Storage Disease Type Ib - Case Report
[2011]
Kavečan, Ivana A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population.
[2017]
Perić, Stojan Genetic Polymorphism of glutathione S-transferases M1, T1 and P1 and susceptibility to oxidative stress and atherogenesis [2012]
I Grubiša; P Otašević; M Dimković; Dedić, VelimirOne small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humans [2017]
Howard, Heidi C.; van, El Carla G.; Forzano, Francesca; Radojković, DragicaФилтери
По типу
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