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Autori: Brinkmann Julia

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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 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  
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