@ARTICLE{
author={Aleksic Dejan Z,Gazdic-Jankovic Marina M,Todorovic Stefan,Kovacevic Marija B,Borkovic Milan P},
year={2023},
title={The first case of combined oxidative phosphorylation deficiency-1 due to a GFM1 mutation in the Serbian population: a case report and literature review},
journal={TURKISH JOURNAL OF PEDIATRICS},
volume={65},
number={6},
pages={1018-1024},
document_type={Article},
} 

@ARTICLE{
author={Borkovic Milan P,Cuturilo Goran,Cerovac Natasa M},
year={2022},
title={Ring chromosome 20: a further contribution to the delineation of epileptic phenotype},
journal={VOJNOSANITETSKI PREGLED},
volume={79},
number={2},
pages={196-200},
document_type={Article},
} 

@ARTICLE{
author={Aleksic Dejan Z,Borkovic Milan P,Krivacic Jelena,Petrusic Igor P,Milic-Rasic Vedrana M},
year={2021},
title={Frameshift Mutation in Polar Rich Domain (PRD) of PQBP1 Gene Associated with Asymmetric Cerebellar Hemispheres: A Case Report of Renpenning Syndrome},
journal={IRANIAN JOURNAL OF PEDIATRICS},
volume={31},
number={4},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Cerovac Natasa M,Terzic Milan M,Borkovic Milan P,Divac Nevena,Stojanovic Radan M,Prostran Milica S},
year={2016},
title={Prenatal diagnosis of lissencephaly: A case report},
journal={VOJNOSANITETSKI PREGLED},
volume={73},
number={1},
pages={77-82},
document_type={Article},
}