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Cardiology in the Young|June 22, 2012
The role of modern imaging techniques in the diagnosis of malposition of the branch pulmonary arteries and possible association with microdeletion 22q11.2Goran Cuturilo, Danijela Drakulic, Aleksandar Krstic, et al.Journal of Child Neurology|October 19, 2019
Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual DisabilityJelena Ruml Stojanovic, Aleksandra Miletic, Borut Peterlin, et al.Iranian Journal of Allergy, Asthma, and Immunology|June 17, 2008
Intraoperative anaphylactic shock in a child with no history of type I hypersensitivityMarina Atanasković-Marković, Marija Gavrović-Jankulović, Tanja Cirković Velicković, et al.Indian Pediatrics|October 25, 2016
Improving the Diagnosis of Children with 22q11.2 Deletion Syndrome: A Single-center Experience from SerbiaGoran Cuturilo, Danijela Drakulic, Ida Jovanovic, et al.American Journal of Medical Genetics. Part A|December 23, 2017
The novel RAF1 mutation p.(Gly361Ala) located outside the kinase domain of the CR3 region in two patients with Noonan syndrome, including one with a rare brain tumorFrederike L Harms, Malik Alawi, David J Amor, et al.Pediatric Cardiology|September 24, 2017
The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative OutcomeGoran Cuturilo, Danijela Drakulic, Ida Jovanovic, et al.Human Molecular Genetics|March 6, 2018
PITX2 deficiency and associated human disease: insights from the zebrafish modelKathryn E Hendee, Elena A Sorokina, Sanaa S Muheisen, et al.Journal of Genetic Counseling|August 4, 2015
Clients' Perception of Outcome of Team-Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) QuestionnaireGoran Cuturilo, Olivera Kontic Vucinic, Ivana Novakovic, et al.The Turkish Journal of Pediatrics|December 23, 2015
Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilitiesTatjana Damnjanovic, Goran Cuturilo, Nela Maksimovic, et al.European Journal of Pediatrics|May 8, 2021
Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unitAleksandra Miletic, Jelena Ruml Stojanovic, Vojislav Parezanovic, et al.Pageof 3