Autori: Miletic Aleksandra
| Naslov | What are key parameters for obtaining the most likely clinical diagnosis from the wide phenotypic spectrum of skeletal dysplasia in patients with previously identified disease-causing gene variant (Meeting Abstract) |
| Autori | Mijovic Marija Bukva Bojan Ruml-Stojanovic Jelena Miletic Aleksandra Bosankic Brankica Petrovic Hristina Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2022), vol. 30 br. SUPPL 1, Suppl. 1, str. 181-181 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit (Article) |
| Autori | Miletic Aleksandra Ruml-Stojanovic Jelena Parezanovic Vojislav M Rsovac Snezana Drakulic Danijela D Soldatovic Ivan A Mijovic Marija Bosankic Brankica Petrovic Hristina Borlja Nikola Milivojevic Milena C Marjanovic Ana Marjanovic Ana Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF PEDIATRICS, (2021), vol. 180 br. 10, str. 3219-3227 |
| Projekat | Ministry of Education, Science and Technological Development, Republic of Serbia [451-03-68/2020-14/200042] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Diversification of Serbian-French-English-Spanish Parallel Corpus ParCoLab with Spoken Language Data (Proceedings Paper) |
| Autori | Terzic Dusica Marjanovic Sasa P Stosic Dejan Miletic Aleksandra |
| Info | TEXT, SPEECH, AND DIALOGUE (TSD 2020), (2020), vol. 12284 br. , str. 61-70 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Skeletal dysplasia in the era of genomic testing: first experience of a single genetic outpatient clinic from Serbia (Meeting Abstract) |
| Autori | Mijovic Marija Ruml-Stojanovic Jelena Miletic Aleksandra Bosankic Brankica Janeski Hristina Peterlin Borut Maver Ales Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 831-831 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability (Article) |
| Autori | Ruml-Stojanovic Jelena Miletic Aleksandra Peterlin Borut Maver Ales Mijovic Marija Borlja Nikola Dimitrijevic Brankica Soldatovic Ivan A Cuturilo Goran |
| Info | JOURNAL OF CHILD NEUROLOGY, (2020), vol. 35 br. 2, str. 116-131 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Rare missense TUBGCP5 gene variant in a patient with primary microcephaly (Article) |
| Autori | Maver Ales Cuturilo Goran Kovanda Anja Miletic Aleksandra Peterlin Borut |
| Info | EUROPEAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 62 br. 12, str. - |
| Projekat | ARRS research programme [P3-0326, J3-8205, J3-5506] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Phenotypic overlap between spondyloepimetaphyseal dysplasia with joint laxity type 2 and Morquio syndrome type A: case report (Meeting Abstract) |
| Autori | Mijovic Marija Miletic Aleksandra Janeski Hristina Dimitrijevic Brankica Ruml-Stojanovic Jelena Lukic M Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1299-1300 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Novel mosaic CREBBP mutation in a patient with overlapping clinical features of Rubinstein-Taybi syndrome and Floating-Harbor syndrome (Meeting Abstract) |
| Autori | Ruml-Stojanovic Jelena Mijovic Marija Miletic Aleksandra Dimitrijevic Brankica Peterlin Borut Maver Ales Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 945-945 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Three patients with pyridoxine-dependent epilepsy - psychological, ethical and professional issues in diagnostic approach as a proof of importance of pre and post-test genetic counseling (Meeting Abstract) |
| Autori | Mijovic Marija Miletic Aleksandra Dimitrijevic Brankica Ruml-Stojanovic Jelena Zivanovic M Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 734-735 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Exome sequencing in disclosing causes of unexpected death in child - single genetic center experience (Meeting Abstract) |
| Autori | Mijovic Marija Miletic Aleksandra Dimitrijevic Brankica Peterlin Borut Maver Ales Ruml-Stojanovic Jelena Zivanovic M Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 164-164 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
