@ARTICLE{
author={Mademont-Soler Irene,...,Perovic Dijana,...,Kravljanac Ruzica M,...,Bosankic Brankica,...,Maksimovic Nela S,...,(broj koautora 37)},
year={2026},
title={Insight into Haploinsufficiency of the ERBB4 Gene: Expanding the Spectrum of Associated Phenotypes},
journal={JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@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={Cvetkovic Mirjana,Petrovic Ana,Pavlovic Sonja T,Paripovic Dusan,Milosevski-Lomic Gordana,Gojkovic Ivana,Matijas Kristina,Zdravkovic Vera M,Radovic Tijana,Pavicevic Polina K,Cuturilo Goran,Bosankic Brankica,Spasojevic Brankica B},
year={2025},
title={Diabetes Triggered by Renal Transplantation in Patients with HNF1B Variants-Single Center Experience},
journal={PEDIATRIC TRANSPLANTATION},
volume={29},
number={},
pages={-},
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={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},
}