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Browsing by Author Bosankić, Brankica
Showing results 1 to 6 of 6
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | 22q11.2 microdeletion is the most common genomic abnormality in Serbian newborns with critical congenital heart disease and could be rapidly detected by Multiplex ligation probe amplification analysis | Miletić, Aleksandra; Cuturilo, Goran; Ruml Stojanović, Jelena; Drakulić, Danijela   ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Stevanović, Milena | Conference Paper | Mp. category will be shown later |
| 2025 | Diabetes triggered by renal transplantation in patients with HNF1B variants - Single center experience | Cvetković, Mirjana; Petrović, Ana; Pavlović, Sonja ; Paripović, Dušan ; Miloševski-Lomić, Gordana; Gojković, Ivana; Matijas, Kristina; Zdravković, Vera ; Radović, Tijana; Pavićević, Polina ;
Čuturilo, Goran
; Bosankić, Brankica; Spasojević, Brankica ; | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2025 | Diagnostic challenges in skeletal dysplasia: a clinical overview based on a 10-year retrospective study of single genetic department | Mijović, Marija; Čuturilo, Goran ; Ruml-Stojanović, Jelena ; Mileticć Aleksandra; Bosankić, Brankica; Dedović, Maja; Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2023 | EP06.016 22q11.2 microdeletion is the most common genomic abnormality in Serbian newborns with critical congenital heart disease and could be rapidly detected by Multiplex ligation probe amplification analysis | Miletić, Aleksandra; Cuturilo, Goran; Ruml Stojanović, Jelena; Drakulić, Danijela ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Stevanović, Milena | Conference Paper | Mp. category will be shown later |
| 2021 | Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit | Miletić, Aleksandra; Ruml-Stojanović, Jelena ; Parezanović, Vojislav ; Rsovac, Snežana; Drakulić, Danijela ; Soldatović, Ivan ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Borlja, Nikola;
Milivojević, Milena
; Marjanović, Ana ; Branković, Marija ; Čuturilo, Goran ; | Научни чланак | 21aM21a - Водећи међународни часопис категорије M21a |
| 2025 | The coexistence of APC and FH germline variants: a case report of cooccurrence of two hereditary cancer predisposition syndromes in a single patient | Bosankić, Brankica; Čuturilo, Goran ; Mijović, Marija; Ruml-Stojanović, Jelena ; Miletić, Aleksandra; Dedović, Maja; Branković, Marija | Conference Paper | Mp. category will be shown later |