Autori: Brinkmann Julia
| Naslov | The clinical significance ofA2ML1variants in Noonan syndrome has to be reconsidered (Article) |
| Autori | Brinkmann Julia ... Cuturilo Goran ... (broj koautora 25) |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2021), vol. 29 br. 3, str. 524-527 |
| Projekat | ERN-ITHACA networking; German Federal Ministry of Education and Research-BMBF (German Network for RASopathy Research "GeNeRARe") [FKZ: 01GM1519A]; German Federal Ministry of Education and Research-BMBF (European Joint Programme on Rare Diseases (NSEuroNet |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | The role of A2ML1 variants in Noonan syndrome remains unverified (Meeting Abstract) |
| Autori | Brinkmann Julia ... Cuturilo Goran ... (broj koautora 24) |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 479-479 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | The novel RAF1 mutation p.(Gly361Ala) located outside the kinase domain of the CR3 region in two patients with Noonan syndrome, including one with a rare brain tumor (Article) |
| Autori | Harms Frederike L Alawi Malik Amor David J Tan Tiong Y Cuturilo Goran Lissewski Christina Brinkmann Julia Schanze Denny Kutsche Kerstin Zenker Martin |
| Info | AMERICAN JOURNAL OF MEDICAL GENETICS PART A, (2018), vol. 176 br. 2, str. 470-476 |
| Projekat | BMBF [01GM1519A, 01GM1519E]; Deutsche Forschungsgemeinschaft [KU 1240/9-1, ZE 524/10-1] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
