How to cite this article: Faivre L, Collod-Beroud G, Callewaert B, Child A, Loeys BL, Binquet C, Gautier E, Arbustini E, Mayer K, Arslan-Kirchner M, Kiotsekoglou A, Comeglio P, Grasso M, Beroud C, Bonithon-Kopp C, Claustres M, Stheneur C, Bouchot O, Wolf JE, Robinson PN, Adès L, De Backer J, Coucke P, Francke U, De Paepe A, Boileau C, Jondeau G. 2009. Pathogenic FBN1 mutations in 146 adults not meeting clinical diagnostic criteria for Marfan syndrome: Further delineation of Type 1 fibrillinopathies and focus on patients with an isolated major criterion. Am J Med Genet Part A 149A:854–860.
Pathogenic FBN1 mutations in 146 adults not meeting clinical diagnostic criteria for Marfan syndrome: Further delineation of type 1 fibrillinopathies and focus on patients with an isolated major criterion†
Version of Record online: 7 APR 2009
Copyright © 2009 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 149A, Issue 5, pages 854–860, May 2009
How to Cite
Faivre, L., Collod-Beroud, G., Callewaert, B., Child, A., Loeys, B.L., Binquet, C., Gautier, E., Arbustini, E., Mayer, K., Arslan-Kirchner, M., Kiotsekoglou, A., Comeglio, P., Grasso, M., Beroud, C., Bonithon-Kopp, C., Claustres, M., Stheneur, C., Bouchot, O., Wolf, J.E., Robinson, P.N., Adès, L., De Backer, J., Coucke, P., Francke, U., De Paepe, A., Boileau, C. and Jondeau, G. (2009), Pathogenic FBN1 mutations in 146 adults not meeting clinical diagnostic criteria for Marfan syndrome: Further delineation of type 1 fibrillinopathies and focus on patients with an isolated major criterion. Am. J. Med. Genet., 149A: 854–860. doi: 10.1002/ajmg.a.32809
- Issue online: 23 APR 2009
- Version of Record online: 7 APR 2009
- Manuscript Accepted: 23 JAN 2009
- Manuscript Received: 14 MAY 2008
- French Ministry of Health
- GIS-Maladies Rares and ANR-Maladies Rares 2005
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