Mijovic Marija,Cuturilo Goran,Ruml-Stojanovic Jelena,Brankovic Marija,Miletic A,Bosankic Brankica,Dedovic Maja,Perovic D,Maksimovic N,Damnjanovic Tatjana M (2025) 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, BALKAN JOURNAL OF MEDICAL GENETICS, vol. 28, br. 2, str. 107-112 (Article) 

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 (2021) Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit, EUROPEAN JOURNAL OF PEDIATRICS, vol. 180, br. 10, str. 3219-3227 (Article) 

Ruml-Stojanovic Jelena,Miletic Aleksandra,Peterlin Borut,Maver Ales,Mijovic Marija,Borlja Nikola,Dimitrijevic Brankica,Soldatovic Ivan A,Cuturilo Goran (2020) Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability, JOURNAL OF CHILD NEUROLOGY, vol. 35, br. 2, str. 116-131 (Article) 

Joksic Ivana D,Cuturilo Goran,Jurisic Aleksandar I,Djuricic Slavisa M,Peterlin Borut,Mijovic Marija,Karadzov-Orlic Natasa T,Egic Amira,Milovanovic Zagorka M (2019) Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in Two Siblings, BALKAN JOURNAL OF MEDICAL GENETICS, vol. 22, br. 2, str. 83-87 (Article) 

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 (2017) The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative Outcome, PEDIATRIC CARDIOLOGY, vol. 38, br. 8, str. 1680-1685 (Article) 

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 (2016) Improving the Diagnosis of Children with 22q11.2 Deletion Syndrome: A Single-center Experience from Serbia, INDIAN PEDIATRICS, vol. 53, br. 9, str. 786-789 (Article) 

Rakonjac Marijana,Cuturilo Goran,Stevanovic Milena J,Jovanovic Ida V,Jelicic-Dobrijevic Ljiljana,Mijovic Marija,Drakulic Danijela D (2016) Speech and Language Abilities of Children with the Familial Form of 22q11.2 Deletion Syndrome, GENETIKA-BELGRADE, vol. 48, br. 1, str. 57-72 (Article) 

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 (2016) Clients' Perception of Outcome of Team-Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) Questionnaire, JOURNAL OF GENETIC COUNSELING, vol. 25, br. 1, str. 189-197 (Article)