Ehlers-Danlos arthrochalasia type (VIIA-B) - expanding the phenotype: from prenatal life through adulthood

M. Klaassens, E. Reinstein, Y. Hilhorst-Hofstee, J. J. P. Schrander, F. Malfait, H. Staal, L. C. ten Have, J. Blaauw, H. C. J. Roggeveen, D. Krakow, A. De Paepe, M. A. M. van Steensel, G. Pals, J. M., Jr. Graham, C. T. R. M. Schrander-Stumpel

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)121-130
JournalClinical Genetics
Volume82
Issue number2
DOIs
Publication statusPublished - Aug 2012

Keywords

  • EDS type VII
  • Ehlers
  • Danlos syndrome (EDS)
  • hypermobility
  • (sub)luxations
  • the arthrochalasia type EDS

Cite this

Klaassens, M., Reinstein, E., Hilhorst-Hofstee, Y., Schrander, J. J. P., Malfait, F., Staal, H., ten Have, L. C., Blaauw, J., Roggeveen, H. C. J., Krakow, D., De Paepe, A., van Steensel, M. A. M., Pals, G., Graham, J. M. . J., & Schrander-Stumpel, C. T. R. M. (2012). Ehlers-Danlos arthrochalasia type (VIIA-B) - expanding the phenotype: from prenatal life through adulthood. Clinical Genetics, 82(2), 121-130. https://doi.org/10.1111/j.1399-0004.2011.01758.x