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
Authors
M Mijovic
University Children’s Hospital, Department of Clinical Genetics, Belgrade, Serbia
Faculty of Medicine, University of Belgrade, Belgrade, Serbia
G Cuturilo
University Children’s Hospital, Department of Clinical Genetics, Belgrade, Serbia
Faculty of Medicine, University of Belgrade, Belgrade, Serbia
J Ruml Stojanovic
University Children’s Hospital, Department of Clinical Genetics, Belgrade, Serbia
M Brankovic
University Children’s Hospital, Department of Clinical Genetics, Belgrade, Serbia
A Miletic
University Children’s Hospital, Department of Clinical Genetics, Belgrade, Serbia
B Bosankic
University Children’s Hospital, Department of Clinical Genetics, Belgrade, Serbia
M Dedovic
University Children’s Hospital, Department of Clinical Genetics, Belgrade, Serbia
D Perovic
Faculty of Medicine, University of Belgrade, Belgrade, Serbia
Institute of Human Genetics, Faculty of Medicine, University of Belgrade, Belgrade, Serbia
N Maksimovic
Faculty of Medicine, University of Belgrade, Belgrade, Serbia
Institute of Human Genetics, Faculty of Medicine, University of Belgrade, Belgrade, Serbia
T Damnjanovic
Faculty of Medicine, University of Belgrade, Belgrade, Serbia
Institute of Human Genetics, Faculty of Medicine, University of Belgrade, Belgrade, Serbia
DOI: https://doi.org/10.2478/bjmg-2025-00026 | Journal eISSN: 2199-5761
Language: English
Page range: 107 - 112
Published on: May 14, 2026
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Related subjects:
© 2026 M Mijovic, G Cuturilo, J Ruml Stojanovic, M Brankovic, A Miletic, B Bosankic, M Dedovic, D Perovic, N Maksimovic, T Damnjanovic, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.