еНаука - преглед
Преглед према Аутор Mijović, Marija
Приказ резултата 1 до 7 од 7
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 ![]() ![]() ![]() ![]() | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
2016 | Clients' Perception of Outcome of Team-Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) Questionnaire | Cuturilo, Goran; Kontić-Vucinić, Olivera; Novaković, Ivana ![]() ![]() ![]() ![]()
Belić, Aleksandra; Ljubić, Aleksandar;
| Научни чланак | 22M22 - Рад у истакнутом међ. часопису |
2020 | Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability (✓) | Ruml-Stojanović, Jelena ![]() ![]() ![]() ![]() ![]() | Научни чланак | 22M22 - Рад у истакнутом међ. часопису |
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 ![]() ![]() ![]() ![]() | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
2021 | Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit (✓) | Miletić, Aleksandra; Ruml-Stojanović, Jelena ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 21M21 - Рад у врхунском међ. часопису |
2016 | Speech and language abilities of children with the familial form of 22q11.2 deletion syndrome (✓) | Rakonjac, Marijana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 23M23 - Рад у међ. часопису |
2023 | Three case reports of patients with rare copy number variations in the recurrent 2q11.1-q11.2 region (✓) | Perović, Dijana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Конференцијски рад | Мп категорија ће бити приказана накнадно. |