Researchers
                                    
                                    
                                    
                                        
                                            Perović, Dijana
                                        
                                        
                                    
                                    
                                
                                
                            Type
Date issued
        
        Results 1-20 of 41
        
        
    
                    
                    
                    
                
                
                
                    | Issue Date | Title | Author(s) | Type | Мp-cat. | 
|---|---|---|---|---|
| 2025 | New evidence supporting female protective effect in patients with congenital anomalies and neurodevelopmental disorders![]()  | Maksimović, Nela  | Article | 21M21  | 
| 2025 | Prenatal diagnosis of chromothripsis causing complex chromosomal rearrangement involving chromosomes 5, 7 and 11 leading to TWIST1 deletion and Saethre-Chotzen syndrome![]()  | Joksić, Ivana D.; Toljić, Mina  | Article | 21M21  | 
| 2025 | Chromosomal Microarray in Children Born Small for Gestational Age - Single Center Experience![]()  | Perović, Dijana  | Article | 23M23  | 
| 2024 | Analysis of the association between MMP-8 gene polymorphisms and the occurrence of adverse effects after acute ischemic stroke treated with recombinant tissue plasminogen activator![]()  | Dušanović-Pjević, Marija G.  | Conference Paper | Mp. category will be shown later  | 
| 2024 | Standardized translations of the Lee Chronic GvHD Symptom Scale to 12 European languages: an EU COST Action cGvHD Eurograft project![]()  | Klingen, Gjaerde Lars; ...; Perović, Dijana  | Other | Mp. category will be shown later  | 
| 2024 | Zbirka pitanja iz biologije - za pripremu prijemnog ispita![]()  | Bunjevački, Vera  | Text book | Mp. category will be shown later  | 
| 2024 | Chromosomal microarray analysis in children with syndromic short stature![]()  | Maksimović, Nela  | Conference Paper | Mp. category will be shown later  | 
| 2024 | Genetic polymorphisms and Methotrexate response in patients with rheumatoid arthritis![]()  | Grk, Milka  | Article | 23M23  | 
| 2024 | Diagnostic yield of chromosomal microarray analysis in patients with congenital heart disease![]()  | Damnjanović, Tatjana  | Conference Paper | Mp. category will be shown later  | 
| 2024 | Association of LGALS3 gene polymorphisms with methotrexate treatment efficacy in patients with rheumatoid arthritis![]()  | Maksimović, Nela  | Conference Paper | Mp. category will be shown later  | 
| 2024 | B7 homolog 3 in pancreatic cancer![]()  | Perović, Dijana  | Article | 21aM21a  | 
| 2024 | Enrichment of pathogenic copy number variants on 17q chromosome in patients with skeletal findings![]()  | Perović, Dijana  | Conference Paper | Mp. category will be shown later  | 
| 2023 | Clinical significance of X chromosome copy number variations![]()  | Perović, Dijana  | Conference Paper | Mp. category will be shown later  | 
| 2023 | Prenatal diagnosis of Saethre-Chotzen syndrome caused by TWIST1 microdeletion and complex chromosomal rearrangement involving chromosomes 5, 7 and 11![]()  | Joksić, Ivana  | Conference Paper | Mp. category will be shown later  | 
| 2023 | Parental Stress of Children with Autism Spectrum Disorder During the Coronavirus Pandemic (COVID-19): Experience from Serbia![]()  | Đurić-Zdravković, Aleksandra  | Article | 23M23  | 
| 2023 | Analysis of genome copy number variations in children with developmental speech and language disorders![]()  | Maksimović, Nela  | Conference Paper | Mp. category will be shown later  | 
| 2023 | Three case reports of patients with rare copy number variations in the recurrent 2q11.1-q11.2 region![]()  | Perović, Dijana  | Conference Paper | Mp. category will be shown later  | 
| 2023 | Association of IL-6 rs1800795, but not TNF-α rs1800629, and IL-1β rs16944 polymorphisms’ genotypes with recovery of ischemic stroke patients following thrombolysis![]()  | Dušanović-Pjević, Marija  | Article | 22M22  | 
| 2023 | Study of IL6 and TNF genes polymorphisms as a risk factor for the development of early neurological disorders and subsequent consequences in neonates![]()  | Đuranović, Ana  | Conference Paper | Mp. category will be shown later  | 
| 2023 | Characterization of small supernumerary marker chromosomes by molecular karyotyping![]()  | Perović, Dijana  | Conference Paper | Mp. category will be shown later  | 
                        