This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Dental-craniofacial manifestation and treatment of rare diseases
International Journal of Oral Science Open Access 20 February 2019
-
Exome sequencing identified new mutations in a Marfan syndrome family
Diagnostic Pathology Open Access 31 January 2014
-
Periodontal disease in a patient with Prader-Willi syndrome: a case report
Journal of Medical Case Reports Open Access 28 July 2011
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
References
McKusick, V. A. Heritable Disorders of Connective Tissue 1st edn (Mosby, St Louis, 1956).
Lee, B. et al. Nature 352, 330–334 (1991).
Maslen, C. L., Corson, G. M., Maddox, B. K., Glanville, R. W. & Sakai, L. Y. Nature 352, 334–337 (1991).
Dietz, H. C. et al. Nature 352, 337–339 (1991).
McKusick, V. A. Circulation 11, 321–342 (1955).
Ingram, V. M. Nature 178, 792–794 (1956).
Ingram, V. M. Biochim. biophys. Acta 36, 402–411 (1959).
Byers, P. H. Trends Genet. 6, 293–300 (1990).
Tromp, G., Kuivanierni, H., Shikata, H. & Prockop, D. J. J. biol. Chem. 264, 1349 (1989).
Vissing, H. et al. J. biol. Chem. 264, 18265–18267 (1989).
Hollister, D. W., Godfrey, M., Sakai, L. Y. & Pyeritz, R. E. New Engl. J. Med. 323, 152–159 (1990).
Sakai, L. Y., Keene, D. R. & Engvall, E. J. Cell Biol. 103, 2499–2509 (1986).
Kainulainen, K. et al. New Engl. J. Med. 323, 935–939 (1990).
Dietz, H. C. et al. Genomics 9, 355–361 (1991).
Magenis, R. E., Maslen, C. L., Smith, L., Allen, L. & Sakai, L. Y. Genomics (in the press).
Carson, N. A. J. et al. Arch. Dis. Child. 38, 425–436 (1963).
Schimke, R. N., McKusick, V. A., Huang, T. & Pollack, A. D. J. Am. med. Ass. 193, 711–719 (1965).
Beals, R. K. & Hecht, F. J. Bone Joint Surg. 53, 987–993 (1971).
Hecht, F. & Beals, R. K. Pediatrics 49, 574–579 (1972).
Majumder, P. P., St Jean, P. L., Ferrell, R. E., Webster, M. W. & Steed, D. L. Am. J. hum. Genet. 48, 164–170 (1991).
Gott, V. L., Pyeritz, R. E., Cameron, D. E., Greene, P. S. & McKusick, V. A. Ann. Thoracic Surg. (in the press).
Demak, R. Sports Illustrated 64, 30–35 (1986).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
McKusick, V. The defect in Marfan syndrome. Nature 352, 279–280 (1991). https://doi.org/10.1038/352279a0
Issue Date:
DOI: https://doi.org/10.1038/352279a0
This article is cited by
-
Dental-craniofacial manifestation and treatment of rare diseases
International Journal of Oral Science (2019)
-
Exome sequencing identified new mutations in a Marfan syndrome family
Diagnostic Pathology (2014)
-
A novel conceptual framework for psychiatry: vertically and horizontally integrated approaches to redundancy and pleiotropism that co-exist with a classification of symptom clusters based on DSM-5
Molecular Psychiatry (2013)
-
Periodontal disease in a patient with Prader-Willi syndrome: a case report
Journal of Medical Case Reports (2011)
-
Penetration of left and right atrial wall and aortic root by an Amplatzer atrial septal occluder in a nine year old boy with Marfan syndrome: Case report
Journal of Cardiothoracic Surgery (2008)