еНаука - преглед
Преглед према Аутор Bosankić, Brankica
Приказ резултата 1 до 10 од 10
| Година | Наслов | Аутор(и) | Тип резултата | Мп-кат. |
|---|---|---|---|---|
| 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 | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2025 | A Novel 4.2 kb deletion of the 3'UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3'UTR![]() | Mijović, Marija; Čuturilo, Goran | Naučni članak | 23M23 - Međunarodni časopis kategorije M23 |
| 2026 | Analysis of Copy Number and Sequence Variants Linked to Cardiac Development in Children with Syndromic Congenital Heart Defects![]() | Damnjanović, Tatjana | Naučni članak | 23M23 - Međunarodni časopis kategorije M23 |
| 2025 | Diabetes triggered by renal transplantation in patients with HNF1B variants - Single center experience![]() | Cvetković, Mirjana; Petrović, Ana; Pavlović, Sonja | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2025 | Diagnostic challenges in skeletal dysplasia: a clinical overview based on a 10-year retrospective study of single genetic department![]() | Mijović, Marija; Čuturilo, Goran | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 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 | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2021 | Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit![]() | Miletić, Aleksandra; Ruml-Stojanović, Jelena | Naučni članak | 21aM21a - Vodeći međunarodni časopis kategorije M21a |
| 2026 | Implementation and clinical utility of the GATK gCNV pipeline for rare disease diagnostics using whole exome sequencing | Pavlović, Đorđe | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2026 | Insight into Haploinsufficiency of the ERBB4 Gene: Expanding the Spectrum of Associated Phenotypes![]() | Mademont-Soler, Irene; ...; Perović, Dijana
(broj koautora 37);
| Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 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 | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
