Elias I.E.I.TraboulsiElias I.E.I., Marfan Syndrome [online], A Compendium of Inherited Disorders and the Eye, Oxford University Press / aao.org / Amerykańska Akademia Okulistyki, 8 listopada 2015 [dostęp 2016-08-18](ang.).
FriedrichF.BörgerFriedrichF., Über zwei Fälle von Arachnodaktylie, „Zeitschrift für Kinderheilkunde”, 12 (2-3), 1914, s. 161–184, DOI: 10.1007/BF02222690, ISSN0178-4919(niem.).
BrendanB.LeeBrendanB. i inni, Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes, „Nature”, 352 (6333), 1991, s. 330–334, DOI: 10.1038/352330a0, ISSN0028-0836, PMID: 1852206.
KoichiK.AkutsuKoichiK. i inni, Characteristics in phenotypic manifestations of genetically proved Marfan syndrome in a Japanese population, „American Journal of Cardiology”, 103 (8), 2009, s. 1146–1148, DOI: 10.1016/j.amjcard.2008.12.037, PMID: 19361604.
M.G.M.G.DoyleM.G.M.G. i inni, Intermediate resistance of Streptococcus pneumoniae to penicillin in children in day-care centers, „The Pediatric Infectious Disease Journal”, 11 (10), 1992, s. 831–835, DOI: 10.1097/00006454-199210000-00005, PMID: 1408481 [dostęp 2023-04-06].
R KR.K.BealsR KR.K., FF.HechtFF., Congenital contractural arachnodactyly: a heritable disorder of connective tissue, „J Bone Joint Surg”, 53 (5), 1971, s. 987-993, PMID: 5557609.
BrendanB.LeeBrendanB. i inni, Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes, „Nature”, 352 (6333), 1991, s. 330–334, DOI: 10.1038/352330a0, ISSN0028-0836, PMID: 1852206.
KoichiK.AkutsuKoichiK. i inni, Characteristics in phenotypic manifestations of genetically proved Marfan syndrome in a Japanese population, „American Journal of Cardiology”, 103 (8), 2009, s. 1146–1148, DOI: 10.1016/j.amjcard.2008.12.037, PMID: 19361604.
A.L.A.L.BurridgeA.L.A.L., Marfan syndrome and the 18th dynasty royal family of ancient Egypt. Preliminary research report [Part II], „Paleopathology Newsletter” (111), 2000, s. 8–13, ISSN0148-4737, PMID: 11624649.
H.H.SchwartzH.H., Abraham Lincoln and aortic insufficiency. The declining health of the President, „California Medicine”, 116 (5), 1972, s. 82–84, ISSN0008-1264, PMID: 4565398, PMCID: PMC1518411.
M.G.M.G.DoyleM.G.M.G. i inni, Intermediate resistance of Streptococcus pneumoniae to penicillin in children in day-care centers, „The Pediatric Infectious Disease Journal”, 11 (10), 1992, s. 831–835, DOI: 10.1097/00006454-199210000-00005, PMID: 1408481 [dostęp 2023-04-06].
FriedrichF.BörgerFriedrichF., Über zwei Fälle von Arachnodaktylie, „Zeitschrift für Kinderheilkunde”, 12 (2-3), 1914, s. 161–184, DOI: 10.1007/BF02222690, ISSN0178-4919(niem.).
BrendanB.LeeBrendanB. i inni, Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes, „Nature”, 352 (6333), 1991, s. 330–334, DOI: 10.1038/352330a0, ISSN0028-0836, PMID: 1852206.
A.L.A.L.BurridgeA.L.A.L., Marfan syndrome and the 18th dynasty royal family of ancient Egypt. Preliminary research report [Part II], „Paleopathology Newsletter” (111), 2000, s. 8–13, ISSN0148-4737, PMID: 11624649.
H.H.SchwartzH.H., Abraham Lincoln and aortic insufficiency. The declining health of the President, „California Medicine”, 116 (5), 1972, s. 82–84, ISSN0008-1264, PMID: 4565398, PMCID: PMC1518411.