Cameron DE, Vricella LA (2005). "Valve-sparing aortic root replacement in Marfan syndrome". Seminars in Thoracic and Cardiovascular Surgery. Pediatric Cardiac Surgery Annual. 8 (1): 103–111. doi:10.1053/j.pcsu.2005.03.001. PMID15818365.
Van de Velde S, Fillman R, Yandow S (March 2006). "Protrusio acetabuli in Marfan syndrome. History, diagnosis, and treatment". The Journal of Bone and Joint Surgery. American Volume. 88 (3): 639–646. doi:10.2106/JBJS.E.00567. PMID16510833.
Graul-Neumann LM, Kienitz T, Robinson PN, Baasanjav S, Karow B, Gillessen-Kaesbach G, et al. (November 2010). "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 A. 152A (11): 2749–2755. doi:10.1002/ajmg.a.33690. PMID20979188. S2CID26408208.
Fitzgibbons RJ, Forse RA (February 2015). "Clinical practice. Groin hernias in adults". The New England Journal of Medicine. 372 (8): 756–763. doi:10.1056/NEJMcp1404068. PMID25693015.
Kohlmeier L, Gasner C, Bachrach LK, Marcus R (October 1995). "The bone mineral status of patients with Marfan syndrome". Journal of Bone and Mineral Research. 10 (10): 1550–1555. doi:10.1002/jbmr.5650101017. PMID8686512. S2CID23492402.
Cameron DE, Vricella LA (2005). "Valve-sparing aortic root replacement in Marfan syndrome". Seminars in Thoracic and Cardiovascular Surgery. Pediatric Cardiac Surgery Annual. 8 (1): 103–111. doi:10.1053/j.pcsu.2005.03.001. PMID15818365.
Hawass Z, Gad YZ, Ismail S, Khairat R, Fathalla D, Hasan N, et al. (February 2010). "Ancestry and pathology in King Tutankhamun's family". JAMA. 303 (7): 638–647. doi:10.1001/jama.2010.121. PMID20159872.
Van de Velde S, Fillman R, Yandow S (March 2006). "Protrusio acetabuli in Marfan syndrome. History, diagnosis, and treatment". The Journal of Bone and Joint Surgery. American Volume. 88 (3): 639–646. doi:10.2106/JBJS.E.00567. PMID16510833.
Graul-Neumann LM, Kienitz T, Robinson PN, Baasanjav S, Karow B, Gillessen-Kaesbach G, et al. (November 2010). "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 A. 152A (11): 2749–2755. doi:10.1002/ajmg.a.33690. PMID20979188. S2CID26408208.
Fitzgibbons RJ, Forse RA (February 2015). "Clinical practice. Groin hernias in adults". The New England Journal of Medicine. 372 (8): 756–763. doi:10.1056/NEJMcp1404068. PMID25693015.
Kohlmeier L, Gasner C, Bachrach LK, Marcus R (October 1995). "The bone mineral status of patients with Marfan syndrome". Journal of Bone and Mineral Research. 10 (10): 1550–1555. doi:10.1002/jbmr.5650101017. PMID8686512. S2CID23492402.
Greally MT (2010). "Shprintzen-Goldberg". In Pagon RA, Bird TD, Dolan CR, et al. (eds.). GeneReviews™ [Internet] (1993–). Seattle WA: University of Washington, Seattle. PMID20301454. NBK1277. Archived from the original on 2021-05-30. Retrieved 2012-04-29.
Cameron DE, Vricella LA (2005). "Valve-sparing aortic root replacement in Marfan syndrome". Seminars in Thoracic and Cardiovascular Surgery. Pediatric Cardiac Surgery Annual. 8 (1): 103–111. doi:10.1053/j.pcsu.2005.03.001. PMID15818365.
Hawass Z, Gad YZ, Ismail S, Khairat R, Fathalla D, Hasan N, et al. (February 2010). "Ancestry and pathology in King Tutankhamun's family". JAMA. 303 (7): 638–647. doi:10.1001/jama.2010.121. PMID20159872.
Greally MT (2010). "Shprintzen-Goldberg". In Pagon RA, Bird TD, Dolan CR, et al. (eds.). GeneReviews™ [Internet] (1993–). Seattle WA: University of Washington, Seattle. PMID20301454. NBK1277. Archived from the original on 2021-05-30. Retrieved 2012-04-29.
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]". Bulletins et Mémoires de la Société Médicale des Hôpitaux de Paris (in French). 13 (3rd series): 220–226. OCLC493643386. NAID10014879958.
Graul-Neumann LM, Kienitz T, Robinson PN, Baasanjav S, Karow B, Gillessen-Kaesbach G, et al. (November 2010). "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 A. 152A (11): 2749–2755. doi:10.1002/ajmg.a.33690. PMID20979188. S2CID26408208.
Kohlmeier L, Gasner C, Bachrach LK, Marcus R (October 1995). "The bone mineral status of patients with Marfan syndrome". Journal of Bone and Mineral Research. 10 (10): 1550–1555. doi:10.1002/jbmr.5650101017. PMID8686512. S2CID23492402.
Greally MT (2010). "Shprintzen-Goldberg". In Pagon RA, Bird TD, Dolan CR, et al. (eds.). GeneReviews™ [Internet] (1993–). Seattle WA: University of Washington, Seattle. PMID20301454. NBK1277. Archived from the original on 2021-05-30. Retrieved 2012-04-29.
Cameron DE, Vricella LA (2005). "Valve-sparing aortic root replacement in Marfan syndrome". Seminars in Thoracic and Cardiovascular Surgery. Pediatric Cardiac Surgery Annual. 8 (1): 103–111. doi:10.1053/j.pcsu.2005.03.001. PMID15818365.
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]". Bulletins et Mémoires de la Société Médicale des Hôpitaux de Paris (in French). 13 (3rd series): 220–226. OCLC493643386. NAID10014879958.