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eNauka >  Results >  Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies
Title: Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies
Authors: Ilenia Maini; Ivan Ivanovski; Đurić, Olivera S. ; Stefano Giuseppe Caraffi; Edoardo Errichiello; Maria Marinelli; Fabrizia Franchi; Veronica Bizzarri; Simonetta Rosato; Marzia Pollazzon;
Chiara Gelmini; Michela Malacarne; Carlo Fusco; Giancarlo Gargano; Sergio Bernasconi; Orsetta Zuffardi; Livia Garavelli;
Issue Date: 2018
Publication: Italian Journal of Pediatrics
ISSN: 1720-8424 Italian Journal of Pediatrics Search Idenfier
Type: Article
Collation: vol. 44 br. 1 str. 34-34
DOI: 10.1186/s13052-018-0467-z
WoS-ID: 000427280300002
Scopus-ID: 2-s2.0-85043353607
PMID: 29523172
PMCID: PMC5845186
URI: https://enauka.gov.rs/handle/123456789/288879
Metadata source: Migrirano iz RIS podataka
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