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The molecular basis of classical Ehlers-Danlos Syndrome (EDS).

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Chicago
de Paepe, A, F Malfait, S Symoens, B Loeys, Lieve Nuytinck, and P Coucke. 2003. “The Molecular Basis of Classical Ehlers-Danlos Syndrome (EDS).” In American Journal of Human Genetics, 73:2308. CHICAGO: UNIV CHICAGO PRESS.
APA
de Paepe, A, Malfait, F., Symoens, S., Loeys, B., Nuytinck, L., & Coucke, P. (2003). The molecular basis of classical Ehlers-Danlos Syndrome (EDS). AMERICAN JOURNAL OF HUMAN GENETICS (Vol. 73, p. 2308). Presented at the Annual Meeting of the American-Society-of-Human-Genetics, CHICAGO: UNIV CHICAGO PRESS.
Vancouver
1.
de Paepe A, Malfait F, Symoens S, Loeys B, Nuytinck L, Coucke P. The molecular basis of classical Ehlers-Danlos Syndrome (EDS). AMERICAN JOURNAL OF HUMAN GENETICS. CHICAGO: UNIV CHICAGO PRESS; 2003. p. 2308.
MLA
de Paepe, A et al. “The Molecular Basis of Classical Ehlers-Danlos Syndrome (EDS).” American Journal of Human Genetics. Vol. 73. CHICAGO: UNIV CHICAGO PRESS, 2003. 2308. Print.
@inproceedings{907146,
  author       = {de Paepe, A and Malfait, F and Symoens, S and Loeys, B and Nuytinck, Lieve and Coucke, P},
  booktitle    = {AMERICAN JOURNAL OF HUMAN GENETICS},
  issn         = {0002-9297},
  language     = {eng},
  location     = {LOS ANGELES, CALIFORNIA},
  number       = {5},
  publisher    = {UNIV CHICAGO PRESS},
  title        = {The molecular basis of classical Ehlers-Danlos Syndrome (EDS).},
  volume       = {73},
  year         = {2003},
}

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