Advanced search
1 file | 13.76 MB Add to list
Author
Organization
Keywords
SYNDROME TYPE-VI, BRITTLE CORNEA SYNDROME, TENASCIN-X DEFICIENCY, THUMB-CLUBFOOT SYNDROME, LYSYL HYDROXYLASE DEFICIENCY, OF-THE-LITERATURE, GALACTOSYLTRANSFERASE-I BETA-4GALT-7, CONGENITAL, ADRENAL-HYPERPLASIA, DERMATAN SULFATE BIOSYNTHESIS, LARGE SUBCUTANEOUS, HEMATOMA, Ehlers-Danlos syndromes, heritable connective tissue disorders, collagen

Downloads

  • (...).pdf
    • full text
    • |
    • UGent only
    • |
    • PDF
    • |
    • 13.76 MB

Citation

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

MLA
Brady, Angela F, Serwet Demirdas, Sylvie Fournel-Gigleux, et al. “The Ehlers-Danlos Syndromes, Rare Types.” AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS 175.1 (2017): 70–115. Print.
APA
Brady, A. F., Demirdas, S., Fournel-Gigleux, S., Ghali, N., Giunta, C., Kapferer-Seebacher, I., Kosho, T., et al. (2017). The Ehlers-Danlos syndromes, rare types. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 175(1), 70–115.
Chicago author-date
Brady, Angela F, Serwet Demirdas, Sylvie Fournel-Gigleux, Neeti Ghali, Cecilia Giunta, Ines Kapferer-Seebacher, Tomoki Kosho, et al. 2017. “The Ehlers-Danlos Syndromes, Rare Types.” American Journal of Medical Genetics Part C-seminars in Medical Genetics 175 (1): 70–115.
Chicago author-date (all authors)
Brady, Angela F, Serwet Demirdas, Sylvie Fournel-Gigleux, Neeti Ghali, Cecilia Giunta, Ines Kapferer-Seebacher, Tomoki Kosho, Roberto Mendoza-Londono, Michael F Pope, Marianne Rohrbach, Tim Van Damme, Anthony Vandersteen, Caroline Van Mourik, Nicol Voermans, Johannes Zschocke, and Fransiska Malfait. 2017. “The Ehlers-Danlos Syndromes, Rare Types.” American Journal of Medical Genetics Part C-seminars in Medical Genetics 175 (1): 70–115.
Vancouver
1.
Brady AF, Demirdas S, Fournel-Gigleux S, Ghali N, Giunta C, Kapferer-Seebacher I, et al. The Ehlers-Danlos syndromes, rare types. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. 2017;175(1):70–115.
IEEE
[1]
A. F. Brady et al., “The Ehlers-Danlos syndromes, rare types,” AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, vol. 175, no. 1, pp. 70–115, 2017.
@article{8529625,
  author       = {Brady, Angela F and Demirdas, Serwet and Fournel-Gigleux, Sylvie and Ghali, Neeti and Giunta, Cecilia and Kapferer-Seebacher, Ines and Kosho, Tomoki and Mendoza-Londono, Roberto and Pope, Michael F and Rohrbach, Marianne and Van Damme, Tim and Vandersteen, Anthony and Van Mourik, Caroline and Voermans, Nicol and Zschocke, Johannes and Malfait, Fransiska},
  issn         = {1552-4868},
  journal      = {AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS},
  keywords     = {SYNDROME TYPE-VI,BRITTLE CORNEA SYNDROME,TENASCIN-X DEFICIENCY,THUMB-CLUBFOOT SYNDROME,LYSYL HYDROXYLASE DEFICIENCY,OF-THE-LITERATURE,GALACTOSYLTRANSFERASE-I BETA-4GALT-7,CONGENITAL,ADRENAL-HYPERPLASIA,DERMATAN SULFATE BIOSYNTHESIS,LARGE SUBCUTANEOUS,HEMATOMA,Ehlers-Danlos syndromes,heritable connective tissue disorders,collagen},
  language     = {eng},
  number       = {1},
  pages        = {70--115},
  title        = {The Ehlers-Danlos syndromes, rare types},
  url          = {http://dx.doi.org/10.1002/ajmg.c.31550},
  volume       = {175},
  year         = {2017},
}

Altmetric
View in Altmetric
Web of Science
Times cited: