«Medical management of Marfan syndrome». Circulation117 (21): 2802–2813. May 2008. doi:10.1161/CIRCULATIONAHA.107.693523. PMID18506019. «estimated prevalence of 1 case per 3000 to 5000 individuals».
«Protrusio acetabuli in Marfan syndrome. History, diagnosis, and treatment». The Journal of Bone and Joint Surgery. American Volume88 (3): 639–646. March 2006. doi:10.2106/JBJS.E.00567. PMID16510833.
«Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3' terminus of the FBN1-gene». American Journal of Medical Genetics. Part A152A (11): 2749–2755. November 2010. doi:10.1002/ajmg.a.33690. PMID20979188.
«Neonatal progeroid variant of Marfan syndrome with congenital lipodystrophy results from mutations at the 3' end of FBN1 gene». European Journal of Medical Genetics57 (5): 230–234. April 2014. doi:10.1016/j.ejmg.2014.02.012. PMID24613577.
«Clinical practice. Groin hernias in adults». The New England Journal of Medicine372 (8): 756–763. February 2015. doi:10.1056/NEJMcp1404068. PMID25693015.
«The bone mineral status of patients with Marfan syndrome». Journal of Bone and Mineral Research10 (10): 1550–1555. October 1995. doi:10.1002/jbmr.5650101017. PMID8686512.
«Personalized external aortic root support: a review of the current status». European Journal of Cardio-Thoracic Surgery50 (3): 400–404. September 2016. doi:10.1093/ejcts/ezw078. PMID27032474.
«Preimplantation genetic testing for Marfan syndrome». Molecular Human Reproduction2 (9): 713–715. September 1996. doi:10.1093/molehr/2.9.713. PMID9239687.
«Medical management of Marfan syndrome». Circulation117 (21): 2802–2813. May 2008. doi:10.1161/CIRCULATIONAHA.107.693523. PMID18506019. «estimated prevalence of 1 case per 3000 to 5000 individuals».
«Protrusio acetabuli in Marfan syndrome. History, diagnosis, and treatment». The Journal of Bone and Joint Surgery. American Volume88 (3): 639–646. March 2006. doi:10.2106/JBJS.E.00567. PMID16510833.
«[The Marfan syndrome and related connective tissue disorders]». Medizinische Monatsschrift Fur Pharmazeuten32 (6): 213–219. June 2009. PMID19554831.
«Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3' terminus of the FBN1-gene». American Journal of Medical Genetics. Part A152A (11): 2749–2755. November 2010. doi:10.1002/ajmg.a.33690. PMID20979188.
«Neonatal progeroid variant of Marfan syndrome with congenital lipodystrophy results from mutations at the 3' end of FBN1 gene». European Journal of Medical Genetics57 (5): 230–234. April 2014. doi:10.1016/j.ejmg.2014.02.012. PMID24613577.
«Clinical practice. Groin hernias in adults». The New England Journal of Medicine372 (8): 756–763. February 2015. doi:10.1056/NEJMcp1404068. PMID25693015.
«The bone mineral status of patients with Marfan syndrome». Journal of Bone and Mineral Research10 (10): 1550–1555. October 1995. doi:10.1002/jbmr.5650101017. PMID8686512.
«Personalized external aortic root support: a review of the current status». European Journal of Cardio-Thoracic Surgery50 (3): 400–404. September 2016. doi:10.1093/ejcts/ezw078. PMID27032474.
«Preimplantation genetic testing for Marfan syndrome». Molecular Human Reproduction2 (9): 713–715. September 1996. doi:10.1093/molehr/2.9.713. PMID9239687.
«Marfan syndrome». Genetics Home Reference. U.S. National Institute of Health. Αρχειοθετήθηκε από το πρωτότυπο στις 29 Αυγούστου 2009. Ανακτήθηκε στις 28 Αυγούστου 2009.
«Marfan syndrome». Genetics Home Reference. U.S. National Institute of Health. Αρχειοθετήθηκε από το πρωτότυπο στις 29 Αυγούστου 2009. Ανακτήθηκε στις 28 Αυγούστου 2009.
Marfan, Antoine (1896). «Un cas de déformation congénitale des quartre membres, plus prononcée aux extrémitiés, caractérisée par l'allongement des os avec un certain degré d'amincissement [A case of congenital deformation of the four limbs, more pronounced at the extremities, characterized by elongation of the bones with some degree of thinning]» (στα γαλλικά). Bulletins et Mémoires de la Société Médicale des Hôpitaux de Paris13 (3rd series): 220–226. Πρότυπο:NAID. OCLC493643386.