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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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