Advanced search
1 file | 257.90 KB

Clinical utility gene card for: hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches

Author
Organization
Keywords
PHENOTYPE, LOEYS-DIETZ SYNDROME, INDIVIDUALS, DISEASE, MUTATIONS, MANAGEMENT, MARFAN-SYNDROME

Downloads

  • (...).pdf
    • full text
    • |
    • UGent only
    • |
    • PDF
    • |
    • 257.90 KB

Citation

Please use this url to cite or link to this publication:

Chicago
Arslan-Kirchner, Mine, Eloisa Arbustini, Catherine Boileau, Philippe Charron, Anne H Child, Gwenaelle Collod-Beroud, Julie De Backer, et al. 2016. “Clinical Utility Gene Card for: Hereditary Thoracic Aortic Aneurysm and Dissection Including Next-generation Sequencing-based Approaches.” European Journal of Human Genetics.
APA
Arslan-Kirchner, M., Arbustini, E., Boileau, C., Charron, P., Child, A. H., Collod-Beroud, G., De Backer, J., et al. (2016). Clinical utility gene card for: hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches. EUROPEAN JOURNAL OF HUMAN GENETICS.
Vancouver
1.
Arslan-Kirchner M, Arbustini E, Boileau C, Charron P, Child AH, Collod-Beroud G, et al. Clinical utility gene card for: hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches. EUROPEAN JOURNAL OF HUMAN GENETICS. 2016. p. 146–50.
MLA
Arslan-Kirchner, Mine, Eloisa Arbustini, Catherine Boileau, et al. “Clinical Utility Gene Card for: Hereditary Thoracic Aortic Aneurysm and Dissection Including Next-generation Sequencing-based Approaches.” EUROPEAN JOURNAL OF HUMAN GENETICS 2016 : 146–150. Print.
@misc{7052445,
  author       = {Arslan-Kirchner, Mine and Arbustini, Eloisa and Boileau, Catherine and Charron, Philippe and Child, Anne H and Collod-Beroud, Gwenaelle and De Backer, Julie and De Paepe, Anne and Dierking, Anna and Faivre, Laurence and Hoffjan, Sabine and Jondeau, Guillaume and Keyser, Britta and Loeys, Bart and Mayer, Karin and Robinson, Peter N and Schmidtke, J{\"o}rg},
  issn         = {1018-4813},
  keyword      = {PHENOTYPE,LOEYS-DIETZ SYNDROME,INDIVIDUALS,DISEASE,MUTATIONS,MANAGEMENT,MARFAN-SYNDROME},
  language     = {eng},
  number       = {1},
  pages        = {146--150},
  series       = {EUROPEAN JOURNAL OF HUMAN GENETICS},
  title        = {Clinical utility gene card for: hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches},
  url          = {http://dx.doi.org/10.1038/ejhg.2015.225},
  volume       = {24},
  year         = {2016},
}

Altmetric
View in Altmetric
Web of Science
Times cited: