Additional file 6: of 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

التفاصيل البيبلوغرافية
العنوان: Additional file 6: of 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
المؤلفون: I. Maini, I. Ivanovski, O. Djuric, S. Caraffi, E. Errichiello, M. Marinelli, F. Franchi, V. Bizzarri, S. Rosato, M. Pollazzon, C. Gelmini, M. Malacarne, C. Fusco, G. Gargano, S. Bernasconi, O. Zuffardi, L. Garavelli
بيانات النشر: figshare, 2018.
سنة النشر: 2018
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, cardiovascular system, cardiovascular diseases
الوصف: Table S6. Correlations between clinical and phenotypic features and aCGH results (likely pathogenic VOUS vs likely benign VOUS + negative aCGH). Statistically significant results for likely pathogenic VOUS are reported in bold [n/N, number of cases with positive variable/number of patients with available data on that variable; NA: not applicable; ADHD: Attention deficit and hyperactivity disorder; ASD: atrial septal defect; CNS: central nervous system; CTG: fetal cardiotocography; IUGR: intrauterine growth restriction; PDA: patent ductus arteriosus; PFO: patent foramen ovale; ToF: Tetralogy of Fallot; VSD: interventricular septal defect]. (DOC 170Â kb)
DOI: 10.6084/m9.figshare.5969923.v1
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a3d766b15c80db90e50e9ff3581313d
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....5a3d766b15c80db90e50e9ff3581313d
قاعدة البيانات: OpenAIRE
الوصف
DOI:10.6084/m9.figshare.5969923.v1