Istraživači
Radivojević, Danijela
Type
Date issued
Results 1-4 of 4
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2024 | Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity? | Ilić, Nikola A.; Marić, Nina; Maver, Aleš; Armengol, Lluis; Kravljanac, Ružica M.   ; Ćirković, Jana; Krstić, Jovana; Radivojević, Danijela ; Ćirković, Sanja S.; Ostojić, Slavica B.;
Krasić, Staša D.; Paripović, Aleksandra; Vukomanović, Vladislav A.
; Peterlin, Borut; Marić, Gorica D. ; Sarajlija, Adrijan ; | Article | 22M22 |
| 2017 | Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature | Aguilera, Cinthia; Vinas-Jornet, Marina; Baena, Neus; Gabau, Elisabeth; Fernandez, Concepcion; Capdevila, Nuria; Ćirković, Sanja S.; Sarajlija, Adrijan ; Mišković, Marijana; Radivojević, Danijela ;
Ruiz, Anna; Guitart, Miriam;
| Article | 22M22 |
| 2017 | The presence of premutation in the FMR1 gene in patients with clinical picture of degenerative ataxia, tremor and parkinsonism | Pešić, Milica ; Marjanović, Ana ; Radivojević, Danijela ; Ćirković, Sanja; Grk, Milka ; Dušanović-Pjević, Marija ; Novaković, Ivana ; Dobričić, Valerija ; Dragašević-Mišković, Nataša ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2013 | Newborn screening for cystic fibrosis in Serbia: A pilot study | Radivojević, Danijela ; Sovtić, Aleksandar ; Minić, Predrag ; Grković, Sanja; Guć-Šćekić, Marija ; Lalić, Tanja; Mišković, Marijana | Article | 22M22 |