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Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes

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BETA RECEPTOR, MARFAN-SYNDROME, MUTATIONS, IDENTIFICATION

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Chicago
Arslan-Kirchner, Mine, Joerg T Epplen, Laurence Faivre, Guillaume Jondeau, Joerg Schmidtke, Anne De Paepe, and Bart Loeys. 2011. “Clinical Utility Gene Card for: Loeys-Dietz Syndrome (TGFBR1/2) and Related Phenotypes.” European Journal of Human Genetics.
APA
Arslan-Kirchner, M., Epplen, J. T., Faivre, L., Jondeau, G., Schmidtke, J., De Paepe, A., & Loeys, B. (2011). Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes. EUROPEAN JOURNAL OF HUMAN GENETICS.
Vancouver
1.
Arslan-Kirchner M, Epplen JT, Faivre L, Jondeau G, Schmidtke J, De Paepe A, et al. Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes. EUROPEAN JOURNAL OF HUMAN GENETICS. 2011.
MLA
Arslan-Kirchner, Mine, Joerg T Epplen, Laurence Faivre, et al. “Clinical Utility Gene Card for: Loeys-Dietz Syndrome (TGFBR1/2) and Related Phenotypes.” EUROPEAN JOURNAL OF HUMAN GENETICS 2011 : n. pag. Print.
@misc{2009512,
  author       = {Arslan-Kirchner, Mine and Epplen, Joerg T and Faivre, Laurence and Jondeau, Guillaume and Schmidtke, Joerg and De Paepe, Anne and Loeys, Bart},
  issn         = {1018-4813},
  keyword      = {BETA RECEPTOR,MARFAN-SYNDROME,MUTATIONS,IDENTIFICATION},
  language     = {eng},
  number       = {10},
  pages        = {4},
  series       = {EUROPEAN JOURNAL OF HUMAN GENETICS},
  title        = {Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes},
  url          = {http://dx.doi.org/10.1038/ejhg.2011.68},
  volume       = {19},
  year         = {2011},
}

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