@ARTICLE{
author={Brinkmann Julia,...,Cuturilo Goran,...,(broj koautora 25)},
year={2021},
title={The clinical significance ofA2ML1variants in Noonan syndrome has to be reconsidered},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={29},
number={3},
pages={524-527},
document_type={Article},
} 

@ARTICLE{
author={Brinkmann Julia,...,Cuturilo Goran,...,(broj koautora 24)},
year={2020},
title={The role of A2ML1 variants in Noonan syndrome remains unverified},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={28},
number={SUPPL 1},
pages={479-479},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Harms Frederike L,Alawi Malik,Amor David J,Tan Tiong Y,Cuturilo Goran,Lissewski Christina,Brinkmann Julia,Schanze Denny,Kutsche Kerstin,Zenker Martin},
year={2018},
title={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},
journal={AMERICAN JOURNAL OF MEDICAL GENETICS PART A},
volume={176},
number={2},
pages={470-476},
document_type={Article},
}