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Genetic analysis of polymorphisms in biologically relevant candidate genes in patients with abdominal aortic aneurysms. J Vasc Surg 2005; 41: 1036\u201342.","DOI":"10.1016\/j.jvs.2005.02.020"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2) Sandford RM, Bown MJ, London NJ, et al. The genetic basis of abdominal aortic aneurysms: a review. Eur J Vasc Endovasc Surg 2007; 33: 381\u201390.","DOI":"10.1016\/j.ejvs.2006.10.025"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3) Albornoz G, Coady MA, Roberts M, et al. Familial thoracic aortic aneurysms and dissections: incidence, modes of inheritance, and phenotypic patterns. Ann Thorac Surg 2006; 82: 1400\u20135.","DOI":"10.1016\/j.athoracsur.2006.04.098"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4) Renard M, Francis C, Ghosh R, et al. Clinical validity of genes for eritable thoracic aortic aneurysm and dissection. 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Mutations in a TGF-beta ligand, TGFB3, cause syndromic aortic aneurysms and dissections. J Am Coll Cardiol 2015; 65: 1324\u201336.","DOI":"10.1016\/j.jacc.2015.01.040"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13) Schepers D, Tortora G, Morisaki H, et al. A mutation update on the LDS-associated genes TGFB2\/3 and SMAD2\/3. Hum Mutat 2018; 39: 621\u201334.","DOI":"10.1002\/humu.23407"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14) Byers PH, Belmont J, Black J, et al. Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome. Am J Med Genet C Semin Med Genet 2017; 175: 40\u20137.","DOI":"10.1002\/ajmg.c.31553"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15) Regalado ES, Mellor-Crummey L, De Backer J, et al. Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations. 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