@article{c9c2855717e64e8dba50fa78cf475164,
title = "Aortic dilation in Sotos syndrome: An underestimated feature?",
keywords = "losartan, adult, aortic disease, aortic root, atrioventricular block, cardiovascular magnetic resonance, case report, child, clinical article, computer assisted tomography, echocardiography, follow up, human, karyotype, Letter, Loeys Dietz syndrome, male, Marfan syndrome, patent ductus arteriosus, preschool child, priority journal, scoring system, Sotos syndrome",
author = "L. Pezzani and L. Mauri and A. Selicorni and A. Peron and M. Grasso and A.C. Codazzi and A. Rimini and P.G. Marchisio and D. Coviello and A. Colli and D. Milani",
note = "Export Date: 5 August 2020 CODEN: AJMGD Correspondence Address: Pezzani, L.; Unit{\`a} di Pediatria ad Alta Intensit{\`a} di Cura, Fondazione IRCCS Ca' Granda, Laboratorio di Genetica Medica, ASST Papa Giovanni XXIIIItaly; email: lidiapezzani@yahoo.it",
year = "2020",
doi = "10.1002/ajmg.a.61591",
language = "English",
volume = "182",
pages = "1819--1823",
journal = "Am. J. Med. Genet. Part A",
issn = "1552-4825",
publisher = "Wiley-Liss Inc.",
number = "7",
}