Advanced search
Add to list

Loss of galactosyltransferase II, encoded by B3GALT6, causes skeletal abnormalities in a zebrafish model for spondylodysplastic Ehlers-Danlos syndrome, the B3GALT6 type

Sarah Delbaere (UGent) , Andy Willaert (UGent) , Phil L Salmon, Paul Coucke (UGent) and Fransiska Malfait (UGent)
Author
Organization

Citation

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

MLA
Delbaere, Sarah et al. “Loss of Galactosyltransferase II, Encoded by B3GALT6, Causes Skeletal Abnormalities in a Zebrafish Model for Spondylodysplastic Ehlers-Danlos Syndrome, the B3GALT6 Type.” Research Day & Student Research Symposium. Ghent, Belgium: Ghent University. Faculty of Medicine and Health Sciences ; Faculty of Pharmaceutical Sciences, 2018. Print.
APA
Delbaere, S., Willaert, A., Salmon, P. L., Coucke, P., & Malfait, F. (2018). Loss of galactosyltransferase II, encoded by B3GALT6, causes skeletal abnormalities in a zebrafish model for spondylodysplastic Ehlers-Danlos syndrome, the B3GALT6 type. Research Day & Student Research Symposium. Presented at the Research Day & Student Research Symposium, Ghent, Belgium: Ghent University. Faculty of Medicine and Health Sciences ; Faculty of Pharmaceutical Sciences.
Chicago author-date
Delbaere, Sarah, Andy Willaert, Phil L Salmon, Paul Coucke, and Fransiska Malfait. 2018. “Loss of Galactosyltransferase II, Encoded by B3GALT6, Causes Skeletal Abnormalities in a Zebrafish Model for Spondylodysplastic Ehlers-Danlos Syndrome, the B3GALT6 Type.” In Research Day & Student Research Symposium. Ghent, Belgium: Ghent University. Faculty of Medicine and Health Sciences ; Faculty of Pharmaceutical Sciences.
Chicago author-date (all authors)
Delbaere, Sarah, Andy Willaert, Phil L Salmon, Paul Coucke, and Fransiska Malfait. 2018. “Loss of Galactosyltransferase II, Encoded by B3GALT6, Causes Skeletal Abnormalities in a Zebrafish Model for Spondylodysplastic Ehlers-Danlos Syndrome, the B3GALT6 Type.” In Research Day & Student Research Symposium. Ghent, Belgium: Ghent University. Faculty of Medicine and Health Sciences ; Faculty of Pharmaceutical Sciences.
Vancouver
1.
Delbaere S, Willaert A, Salmon PL, Coucke P, Malfait F. Loss of galactosyltransferase II, encoded by B3GALT6, causes skeletal abnormalities in a zebrafish model for spondylodysplastic Ehlers-Danlos syndrome, the B3GALT6 type. Research Day & Student Research Symposium. Ghent, Belgium: Ghent University. Faculty of Medicine and Health Sciences ; Faculty of Pharmaceutical Sciences; 2018.
IEEE
[1]
S. Delbaere, A. Willaert, P. L. Salmon, P. Coucke, and F. Malfait, “Loss of galactosyltransferase II, encoded by B3GALT6, causes skeletal abnormalities in a zebrafish model for spondylodysplastic Ehlers-Danlos syndrome, the B3GALT6 type,” in Research Day & Student Research Symposium, Ghent, Belgium, 2018.
@inproceedings{8602846,
  author       = {Delbaere, Sarah and Willaert, Andy and Salmon, Phil L and Coucke, Paul and Malfait, Fransiska},
  booktitle    = {Research Day & Student Research Symposium},
  language     = {eng},
  location     = {Ghent, Belgium},
  publisher    = {Ghent University. Faculty of Medicine and Health Sciences ; Faculty of Pharmaceutical Sciences},
  title        = {Loss of galactosyltransferase II, encoded by B3GALT6, causes skeletal abnormalities in a zebrafish model for spondylodysplastic Ehlers-Danlos syndrome, the B3GALT6 type},
  year         = {2018},
}