Autori: Bosankic Brankica
| Naslov | Insight into Haploinsufficiency of the ERBB4 Gene: Expanding the Spectrum of Associated Phenotypes (Article; Early Access) |
| Autori | Mademont-Soler Irene ... Perovic Dijana ... Kravljanac Ruzica M ... Bosankic Brankica ... Maksimovic Nela S ... (broj koautora 37) |
| Info | JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, (2026), vol. br. , str. - |
| Projekat | Fundaci Instituci dels Centres de Recerca de Catalunya (CERCA) |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: |
| Naslov | 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 (Article) |
| Autori | Mijovic Marija Cuturilo Goran Ruml-Stojanovic Jelena Brankovic Marija Miletic A Bosankic Brankica Dedovic Maja Perovic D Maksimovic N Damnjanovic Tatjana M |
| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2025), vol. 28 br. 2, str. 107-112 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
| Naslov | Diagnostic challenges in skeletal dysplasia: a clinical overview based on a 10-year retrospective study of single genetic department (Meeting Abstract) |
| Autori | Mijovic Marija Cuturilo Goran Ruml-Stojanovic Jelena Miletic Aleksandra Bosankic Brankica Dedovic Maja Brankovic Marija |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 668-668 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | The coexistence of APC and FH germline variants: a case report of cooccurrence of two hereditary cancer predisposition syndromes in a single patient (Meeting Abstract) |
| Autori | Bosankic Brankica Cuturilo Goran Mijovic Marija Ruml-Stojanovic Jelena Miletic Aleksandra Dedovic Maja Brankovic Marija |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 563-563 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | Diabetes Triggered by Renal Transplantation in Patients with HNF1B Variants-Single Center Experience (Meeting Abstract) |
| Autori | Cvetkovic Mirjana Petrovic Ana Pavlovic Sonja T Paripovic Dusan Milosevski-Lomic Gordana Gojkovic Ivana Matijas Kristina Zdravkovic Vera M Radovic Tijana Pavicevic Polina K Cuturilo Goran Bosankic Brankica Spasojevic Brankica B |
| Info | PEDIATRIC TRANSPLANTATION, (2025), vol. 29 br. , Suppl. 1, str. - |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | Clinical utility of diagnostic NGS for detection CNV variants in genes associated with skeletal dysplasia (Meeting Abstract) |
| Autori | Mijovic Marija Cuturilo Goran Ruml-Stojanovic Jelena Miletic Aleksandra Bosankic Brankica Petrovic Hristina |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1373-1373 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | Clinical utility of diagnostic NGS for detection CNV variants in genes associated with skeletal dysplasia (Meeting Abstract) |
| Autori | Mijovic Marija Cuturilo Goran Ruml-Stojanovic Jelena Miletic Aleksandra Bosankic Brankica Petrovic Hristina |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1373-1373 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | Dual molecular diagnosis in patients with skeletal dysplasia - data from tertiary genetic center (Meeting Abstract) |
| Autori | Mijovic Marija Cuturilo Goran Ruml-Stojanovic Jelena Miletic Aleksandra Bosankic Brankica Petrovic Hristina Vasic Bojana Vukasinovic Nadja |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 1, str. 412-413 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | Internal Skeletal Dysplasia Registry within the electronic database of Department of Clinical Genetics University Children's Hospital in Belgrade - basis for a personalised medicine in the future (Meeting Abstract) |
| Autori | Mijovic Marija Cuturilo Goran Ruml-Stojanovic Jelena Miletic Aleksandra Bosankic Brankica Petrovic Hristina |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 401-402 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | Constitutional mismatch repair deficiency syndrome (CMMRD): the significance of customized surveillance protocol for Lynch syndrome-related tumors in relatives at risk-a case report (Meeting Abstract) |
| Autori | Bosankic Brankica Cuturilo Goran Petrovic Hristina Mijovic Marija Ruml-Stojanovic Jelena Miletic Aleksandra |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 265-266 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
