These authors contributed equally to this work.
Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation
Version of Record online: 23 SEP 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 86, Issue 3, pages 238–245, September 2014
How to Cite
Sheikhzadeh, S., Sondermann, C., Rybczynski, M., Habermann, C.R., Brockstaedt, L., Keyser, B., Kaemmerer, H., Mir, T., Staebler, A., Robinson, P.N., Kutsche, K., Berger, J., Blankenberg, S. and von Kodolitsch, Y. (2014), Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation. Clinical Genetics, 86: 238–245. doi: 10.1111/cge.12264
There is no conflict of interest to be stated by any of the authors.
- Issue online: 20 AUG 2014
- Version of Record online: 23 SEP 2013
- Accepted manuscript online: 29 AUG 2013 10:27AM EST
- Manuscript Revised: 26 AUG 2013
- Manuscript Accepted: 26 AUG 2013
- Manuscript Received: 4 JUL 2013
|cge12264-sup-0001-TableS1.doc||Word document||50K||Table S1. The Ghent-1 nosology for diagnosing Marfan syndrome (1).|
|cge12264-sup-0002-TableS2.doc||Word document||46K||Table S2. The Ghent-2 nosology for diagnosing Marfan syndrome (2).|
|cge12264-sup-0003-TableS3.doc||Word document||78K||Table S3. Reported prevalence of dural ectasia on MRI in Marfan patients.|
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