@ARTICLE{
author={Mijovic Marija,Cuturilo Goran,Ruml-Stojanovic Jelena,Brankovic Marija,Miletic A,Bosankic Brankica,Dedovic Maja,Perovic D,Maksimovic N,Damnjanovic Tatjana M},
year={2025},
title={A Novel 4.2 kb deletion of the 3′UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3′UTR},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={28},
number={2},
pages={107-112},
document_type={Article},
} 

@ARTICLE{
author={Mijovic Marija,Cuturilo Goran,Ruml-Stojanovic Jelena,Miletic Aleksandra,Bosankic Brankica,Dedovic Maja,Brankovic Marija},
year={2025},
title={Diagnostic challenges in skeletal dysplasia: a clinical overview based on a 10-year retrospective study of single genetic department},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={668-668},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Bosankic Brankica,Cuturilo Goran,Mijovic Marija,Ruml-Stojanovic Jelena,Miletic Aleksandra,Dedovic Maja,Brankovic Marija},
year={2025},
title={The coexistence of APC and FH germline variants: a case report of cooccurrence of two hereditary cancer predisposition syndromes in a single patient},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={563-563},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mijovic Marija,Cuturilo Goran,Ruml-Stojanovic Jelena,Miletic Aleksandra,Bosankic Brankica,Petrovic Hristina},
year={2024},
title={Clinical utility of diagnostic NGS for detection CNV variants in genes associated with skeletal dysplasia},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1373-1373},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mijovic Marija,Cuturilo Goran,Ruml-Stojanovic Jelena,Miletic Aleksandra,Bosankic Brankica,Petrovic Hristina},
year={2024},
title={Clinical utility of diagnostic NGS for detection CNV variants in genes associated with skeletal dysplasia},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1373-1373},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mijovic Marija,Cuturilo Goran,Ruml-Stojanovic Jelena,Miletic Aleksandra,Bosankic Brankica,Petrovic Hristina,Vasic Bojana,Vukasinovic Nadja},
year={2024},
title={Dual molecular diagnosis in patients with skeletal dysplasia - data from tertiary genetic center},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={412-413},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mijovic Marija,Cuturilo Goran,Ruml-Stojanovic Jelena,Miletic Aleksandra,Bosankic Brankica,Petrovic Hristina},
year={2023},
title={Internal Skeletal Dysplasia Registry within the electronic database of Department of Clinical Genetics University Children's Hospital in Belgrade - basis for a personalised medicine in the future},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={401-402},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Perovic Dijana,Maksimovic Nela S,Damnjanovic Tatjana M,Djuranovic Ana S,Sarajlija Adrijan,Mijovic Marija},
year={2023},
title={Three case reports of patients with rare copy number variations in the recurrent 2q11.1-q11.2 region},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={267-268},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Bosankic Brankica,Cuturilo Goran,Petrovic Hristina,Mijovic Marija,Ruml-Stojanovic Jelena,Miletic Aleksandra},
year={2023},
title={Constitutional mismatch repair deficiency syndrome (CMMRD): the significance of customized surveillance protocol for Lynch syndrome-related tumors in relatives at risk-a case report},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={265-266},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Miletic Aleksandra,Cuturilo Goran,Ruml-Stojanovic Jelena,Drakulic Danijela D,Mijovic Marija,Bosankic Brankica,Petrovic Hristina,Stevanovic Milena J},
year={2023},
title={22q11.2 microdeletion is the most common genomic abnormality in Serbian newborns with critical congenital heart disease and could be rapidly detected by Multiplex ligation probe amplification analysis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={140-140},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Ruml-Stojanovic Jelena,Mijovic Marija,Miletic Aleksandra,Bosankic Brankica,Petrovic Hristina,Cuturilo Goran},
year={2022},
title={Multiple major anomalies and microcephaly predict the detection of pathogenic copy number variations in patients with moderate and severe global developmental delay/intellectual disability},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={30},
number={SUPPL 1},
pages={239-239},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mijovic Marija,Bukva Bojan,Ruml-Stojanovic Jelena,Miletic Aleksandra,Bosankic Brankica,Petrovic Hristina,Cuturilo Goran},
year={2022},
title={What are key parameters for obtaining the most likely clinical diagnosis from the wide phenotypic spectrum of skeletal dysplasia in patients with previously identified disease-causing gene variant},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={30},
number={SUPPL 1},
pages={181-181},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Miletic Aleksandra,Ruml-Stojanovic Jelena,Parezanovic Vojislav M,Rsovac Snezana,Drakulic Danijela D,Soldatovic Ivan A,Mijovic Marija,Bosankic Brankica,Petrovic Hristina,Borlja Nikola,Milivojevic Milena C,Marjanovic Ana,Marjanovic Ana,Cuturilo Goran},
year={2021},
title={Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit},
journal={EUROPEAN JOURNAL OF PEDIATRICS},
volume={180},
number={10},
pages={3219-3227},
document_type={Article},
} 

@ARTICLE{
author={Mijovic Marija,Ruml-Stojanovic Jelena,Miletic Aleksandra,Bosankic Brankica,Janeski Hristina,Peterlin Borut,Maver Ales,Cuturilo Goran},
year={2020},
title={Skeletal dysplasia in the era of genomic testing: first experience of a single genetic outpatient clinic from Serbia},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={28},
number={SUPPL 1},
pages={831-831},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Ruml-Stojanovic Jelena,Miletic Aleksandra,Peterlin Borut,Maver Ales,Mijovic Marija,Borlja Nikola,Dimitrijevic Brankica,Soldatovic Ivan A,Cuturilo Goran},
year={2020},
title={Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability},
journal={JOURNAL OF CHILD NEUROLOGY},
volume={35},
number={2},
pages={116-131},
document_type={Article},
} 

@ARTICLE{
author={Joksic Ivana D,Cuturilo Goran,Jurisic Aleksandar I,Djuricic Slavisa M,Peterlin Borut,Mijovic Marija,Karadzov-Orlic Natasa T,Egic Amira,Milovanovic Zagorka M},
year={2019},
title={Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in Two Siblings},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={22},
number={2},
pages={83-87},
document_type={Article},
} 

@ARTICLE{
author={Mijovic Marija,Miletic Aleksandra,Janeski Hristina,Dimitrijevic Brankica,Ruml-Stojanovic Jelena,Lukic M,Cuturilo Goran},
year={2019},
title={Phenotypic overlap between spondyloepimetaphyseal dysplasia with joint laxity type 2 and Morquio syndrome type A: case report},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={1299-1300},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Ruml-Stojanovic Jelena,Mijovic Marija,Miletic Aleksandra,Dimitrijevic Brankica,Peterlin Borut,Maver Ales,Cuturilo Goran},
year={2019},
title={Novel mosaic CREBBP mutation in a patient with overlapping clinical features of Rubinstein-Taybi syndrome and Floating-Harbor syndrome},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={945-945},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mijovic Marija,Miletic Aleksandra,Dimitrijevic Brankica,Ruml-Stojanovic Jelena,Zivanovic M,Cuturilo Goran},
year={2019},
title={Three patients with pyridoxine-dependent epilepsy - psychological, ethical and professional issues in diagnostic approach as a proof of importance of pre and post-test genetic counseling},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={734-735},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mijovic Marija,Miletic Aleksandra,Dimitrijevic Brankica,Peterlin Borut,Maver Ales,Ruml-Stojanovic Jelena,Zivanovic M,Cuturilo Goran},
year={2019},
title={Exome sequencing in disclosing causes of unexpected death in child - single genetic center experience},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={164-164},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mijovic Marija,Miletic Aleksandra,Ruml-Stojanovic Jelena,Peterlin Borut,Maver Ales,Borlja Nikola,Dimitrijevic Brankica,Lukic M,Cuturilo Goran},
year={2018},
title={A novel CTNNB1 mutation in a patient with teratoma and multiple malformations - expansion of the phenotypic spectrum and possible new gene for Currarino phenotype},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={26},
number={},
pages={465-465},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Cuturilo Goran,Drakulic Danijela D,Jovanovic Ida V,Ilic Slobodan G,Kalanj Jasna,Vulicevic Irena,Raus Misela V,Skoric Dejan,Mijovic Marija,Medjo Biljana P,Rsovac Snezana,Stevanovic Milena J},
year={2017},
title={The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative Outcome},
journal={PEDIATRIC CARDIOLOGY},
volume={38},
number={8},
pages={1680-1685},
document_type={Article},
} 

@ARTICLE{
author={Cuturilo Goran,Drakulic Danijela D,Jovanovic Ida V,Krstic Aleksandar,Djukic Milan M,Skoric Dejan,Mijovic Marija,Stefanovic Igor D,Milivojevic Milena C,Stevanovic Milena J},
year={2016},
title={Improving the Diagnosis of Children with 22q11.2 Deletion Syndrome: A Single-center Experience from Serbia},
journal={INDIAN PEDIATRICS},
volume={53},
number={9},
pages={786-789},
document_type={Article},
} 

@ARTICLE{
author={Rakonjac Marijana,Cuturilo Goran,Stevanovic Milena J,Jovanovic Ida V,Jelicic-Dobrijevic Ljiljana,Mijovic Marija,Drakulic Danijela D},
year={2016},
title={Speech and Language Abilities of Children with the Familial Form of 22q11.2 Deletion Syndrome},
journal={GENETIKA-BELGRADE},
volume={48},
number={1},
pages={57-72},
document_type={Article},
} 

@ARTICLE{
author={Cuturilo Goran,Kontic-Vucinic Olivera,Novakovic Ivana V,Ignjatovic Svetlana D,Mijovic Marija,Sulovic Nenad,Vukolic D,Komnenic Milica,Tadic Jasmina,Cetkovic Aleksandar,Belic Aleksandra,Ljubic Aleksandar D},
year={2016},
title={Clients' Perception of Outcome of Team-Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) Questionnaire},
journal={JOURNAL OF GENETIC COUNSELING},
volume={25},
number={1},
pages={189-197},
document_type={Article},
}