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Disease Markers
Volume 2015 (2015), Article ID 828970, 9 pages
http://dx.doi.org/10.1155/2015/828970
Research Article

Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian Family

Center for Medical Genetics, Ghent University Hospital, 9000 Ghent, Belgium

Received 15 June 2015; Revised 1 September 2015; Accepted 10 September 2015

Academic Editor: Ralf Lichtinghagen

Copyright © 2015 Delfien Syx et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [3 citations]

The following is the list of published articles that have cited the current article.

  • Nicoletta Zoppi, Marina Colombi, Nicola Chiarelli, Giulia Carini, Chiara Dordoni, Marco Ritelli, Marina Venturini, and Marco Castori, “Transcriptome-wide expression profiling in skin fibroblasts of patients with joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type,” PLoS ONE, vol. 11, no. 8, 2016. View at Publisher · View at Google Scholar
  • Robert D. Gerwin, “Benign Joint Hypermobility is not Benign,” Myopain, pp. 1–2, 2016. View at Publisher · View at Google Scholar
  • Brad Tinkle, Marco Castori, Britta Berglund, Helen Cohen, Rodney Grahame, Hanadi Kazkaz, and Howard Levy, “Hypermobile Ehlers-Danlos syndrome (a.k.a. Ehlers-Danlos syndrome Type III and Ehlers-Danlos syndrome hypermobility type): Clinical description and natural history,” American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2017. View at Publisher · View at Google Scholar