Autori: Petrovic Hristina
| 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 | Dihydroquercetin and biochaga reduce H2O2-induced DNA damage in peripheral blood mononuclear cells of obese women in vitro-a pilot study (Article; Early Access) |
| Autori | Zivkovic Lada P Pirkovic Andrea Topalovic Dijana B Borozan Suncica Z Bajic Vladan P Dimitrijevic-Sreckovic Vesna S Djelic Ninoslav J Petrovic Hristina Milic Mirta Spremo-Potparevic Biljana |
| Info | MUTAGENESIS, (2024), vol. br. , str. - |
| Projekat | Ministry of Education, Science and Technological Development, Republic of Serbia; University of Belgrade-Faculty of Pharmacy [451-03-65/2024-03/ 200161, 451-03-66/2024-03/ 200161] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: |
| 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 |
| Naslov | 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 (Meeting Abstract) |
| Autori | Miletic Aleksandra Cuturilo Goran Ruml-Stojanovic Jelena Drakulic Danijela D Mijovic Marija Bosankic Brankica Petrovic Hristina Stevanovic Milena J |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 140-140 |
| Projekat | Ministry of Education, Science and Technological Development of the Republic of Serbia [451-03-68/2020-14/200042]; Serbian Academy of Sciences and Arts |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | Serum leptin levels in children and adolescents with spinal muscular atrophy types 2 and 3 (Article) |
| Autori | Djordjevic Stefan A Milic-Rasic Vedrana M Brankovic Vesna Kosac Ana P Dejanovic-Djordjevic Ivana Bijelic Maja Dimkic-Tomic Tijana J Markovic-Denic Ljiljana N Kovacevic Smiljka Petrovic Hristina Vitorovic S Dobric Z Zdravkovic Vera M |
| Info | ARCHIVES DE PEDIATRIE, (2022), vol. 29 br. 7, str. 480-483 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
| Naslov | Multiple major anomalies and microcephaly predict the detection of pathogenic copy number variations in patients with moderate and severe global developmental delay/intellectual disability (Meeting Abstract) |
| Autori | Ruml-Stojanovic Jelena Mijovic Marija Miletic Aleksandra Bosankic Brankica Petrovic Hristina Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2022), vol. 30 br. SUPPL 1, Suppl. 1, str. 239-239 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| 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 |
