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Browsing by Author Borlja, Nikola
Showing results 1 to 3 of 3
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2018 | A novel CTNNB1 mutation in a patient with teratoma and multiple malformations - expansion of the phenotypic spectrum and possible new gene for Currarino phenotype | Mijovic, Marija; Miletic, Aleksandra; Ruml-Stojanovic, Jelena; Peterlin, Borut; Maver, Ales; Borlja, Nikola; Dimitrijevic, Brankica; Lukic, M; Cuturilo, Goran | Conference Paper | Mp. category will be shown later |
| 2020 | Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability | Ruml-Stojanović, Jelena  ; Miletić, Aleksandra; Peterlin, Borut; Maver, Ales; Mijović, Marija; Borlja, Nikola; Dimitrijević, Brankica; Soldatović, Ivan A.  ; Čuturilo, Goran | Article | 22M22 |
| 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 ; | Article | 21aM21a |