Marija Mijovic
Belgrade, SE, Serbia
Last Updated: 09/26/2026
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Found 11 publications
Two siblings with lipoid congenital adrenal hyperplasia: first reported case in Serbia and literature review.
Journal: Frontiers in endocrinology
Published: June 17, 2026
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 : BJMG
Published: May 18, 2026
Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit.
Journal: European journal of pediatrics
Published: March 18, 2021
Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in two Siblings.
Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in two Siblings.
Journal: Balkan journal of medical genetics : BJMG
Published: January 17, 2020
Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability.
Journal: Journal of child neurology
Published: October 19, 2019
Protective effects of whey on rat liver damage induced by chronic alcohol intake.
Journal: Human & experimental toxicology
Published: February 21, 2019
Toxicity study of DE-EDCP as a potential drug for cancer therapy: Toxicity profile of DE-EDCP.
Journal: Human & experimental toxicology
Published: December 19, 2018
Intraosseous lipoma of the maxillary tuberosity: A case report.
Journal: Journal of stomatology, oral and maxillofacial surgery
Published: May 13, 2017
The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative Outcome.
Journal: Pediatric cardiology
Published: March 12, 2017
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
Published: September 30, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026