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Pediatric Dermatology|September 12, 2014
Ectodermal Defects and Anal Atresia in a Child with a TP63 Mutation--Expanding the Phenotypic SpectrumJelena Ruml, Goran Cuturilo, Marija Lukac, et al.
Indian Pediatrics|January 7, 2015
Wiskott-Aldrich syndrome with macrothrombocytopeniaDejan Skoric, Aleksandar Dimitrijevic, Goran Cuturilo, et al.
Srpski Arhiv Za Celokupno Lekarstvo|September 22, 2009
[Mowat-Wilson syndrome--a case report]Goran Cuturilo, Igor Stefanović, Ida Jovanović, et al.
Indian Pediatrics|August 14, 2012
Inhaled nitric oxide therapy for acute respiratory distress syndrome in childrenBiljana Medjo, Marina Atanaskovic-Markovic, Dimitrije Nikolic, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 31, 2008
Prenatal growth retardation, microcephaly, and eye coloboma in infant with multiple congenital anomalies: further delineation of presumed new dysmorphic syndromeGoran Cuturilo, Ida Jovanovic, Goran Vukomanovic, et al.
Research in Developmental Disabilities|May 29, 2016
Differences in speech and language abilities between children with 22q11.2 deletion syndrome and children with phenotypic features of 22q11.2 deletion syndrome but without microdeletionMarijana Rakonjac, Goran Cuturilo, Milena Stevanovic, et al.
European Journal of Pediatrics|August 12, 2011
4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndromeGoran Cuturilo, Björn Menten, Aleksandar Krstic, et al.
Children (Basel, Switzerland)|April 27, 2024
Speech Sounds Production, Narrative Skills, and Verbal Memory of Children with 22q11.2 MicrodeletionMarijana Rakonjac, Goran Cuturilo, Natasa Kovacevic-Grujicic, et al.
European Journal of Pediatrics|November 28, 2007
A rare association of interrupted aortic arch type C and microdeletion 22q11.2Goran Cuturilo, Danijela Drakulic, Milena Stevanovic, et al.
Srpski Arhiv Za Celokupno Lekarstvo|February 18, 2012
Epilepsy in a child with Wolf-Hirschhorn syndromeVesna Mitić, Goran Cuturilo, Ivana Novaković, et al.
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