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Browsing by Author Bosankić, Brankica

Showing results 1 to 6 of 6
Issue DateTitleAuthor(s)TypeМp-cat.
202322q11.2 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 analysisMiletić, Aleksandra; Cuturilo, Goran; Ruml Stojanović, Jelena; Drakulić, Danijela  ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Stevanović, Milena  Conference Paper
Mp. category will be shown later
2025Diabetes triggered by renal transplantation in patients with HNF1B variants - Single center experienceCvetković, 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.
2025Diagnostic challenges in skeletal dysplasia: a clinical overview based on a 10-year retrospective study of single genetic departmentMijović, Marija; Čuturilo, Goran  ; Ruml-Stojanović, Jelena ; Mileticć Aleksandra; Bosankić, Brankica; Dedović, Maja; Branković, Marija  Conference Paper
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2023EP06.016 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 analysisMiletić, Aleksandra; Cuturilo, Goran; Ruml Stojanović, Jelena; Drakulić, Danijela  ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Stevanović, Milena  Conference Paper
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2021Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unitMiletić, 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
2025The coexistence of APC and FH germline variants: a case report of cooccurrence of two hereditary cancer predisposition syndromes in a single patientBosankić, Brankica; Čuturilo, Goran  ; Mijović, Marija; Ruml-Stojanović, Jelena ; Miletić, Aleksandra; Dedović, Maja; Branković, Marija  Conference Paper
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