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) 

Mijovic Marija,Cuturilo Goran,Ruml-Stojanovic Jelena,Miletic Aleksandra,Bosankic Brankica,Dedovic Maja,Brankovic Marija (2025) Diagnostic challenges in skeletal dysplasia: a clinical overview based on a 10-year retrospective study of single genetic department, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 33, br. , str. 668-668 (Meeting Abstract) 

Bosankic Brankica,Cuturilo Goran,Mijovic Marija,Ruml-Stojanovic Jelena,Miletic Aleksandra,Dedovic Maja,Brankovic Marija (2025) The coexistence of APC and FH germline variants: a case report of cooccurrence of two hereditary cancer predisposition syndromes in a single patient, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 33, br. , str. 563-563 (Meeting Abstract)