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Leveraging consanguinity in inherited retinal diseases uncovers missing genetic variation : rare novel disease genes and a multitude of novel variants in known disease genes

Kristof Van Schil UGent, Sarah Naessens UGent, Stijn Van De Sompele UGent, Nuria Gruartmoner Roura, Marjolein Carron UGent, Katharina Dannhausen, Sarah De Jaegere, Maxim Vanpanteghem, Frauke Coppieters, Marcus Karlstetter, et al. (2017) American Society of Human Genetics, Annual meeting, Abstracts.
Please use this url to cite or link to this publication:
author
organization
year
type
conference (poster)
publication status
published
subject
in
American Society of Human Genetics, Annual meeting, Abstracts
conference name
2017 Annual meeting of the American Society of Human Genetics (ASHG 2017)
conference location
Orlando, FL, USA
conference start
2017-10-17
conference end
2017-10-21
language
English
UGent publication?
yes
classification
C3
id
8555670
handle
http://hdl.handle.net/1854/LU-8555670
date created
2018-03-14 15:44:07
date last changed
2018-05-17 08:55:02
@inproceedings{8555670,
  author       = {Van Schil, Kristof and Naessens, Sarah and Van De Sompele, Stijn and Gruartmoner Roura, Nuria and Carron, Marjolein and Dannhausen, Katharina and De Jaegere, Sarah and Vanpanteghem, Maxim and Coppieters, Frauke and Karlstetter, Marcus and Tsou, Bryan and Langmann, Thomas and Meire, Fran\c{c}oise and Maroofian, Reza and Crosby, Andrew H and Balikova, Irina and Van Lint, Michel and Webster, Andrew and Michaelides, Michel and Leroy, Bart and De Baere, Elfride},
  booktitle    = {American Society of Human Genetics, Annual meeting, Abstracts},
  language     = {eng},
  location     = {Orlando, FL, USA},
  title        = {Leveraging consanguinity in inherited retinal diseases uncovers missing genetic variation : rare novel disease genes and a multitude of novel variants in known disease genes},
  year         = {2017},
}

Chicago
Van Schil, Kristof, Sarah Naessens, Stijn Van De Sompele, Nuria Gruartmoner Roura, Marjolein Carron, Katharina Dannhausen, Sarah De Jaegere, et al. 2017. “Leveraging Consanguinity in Inherited Retinal Diseases Uncovers Missing Genetic Variation : Rare Novel Disease Genes and a Multitude of Novel Variants in Known Disease Genes.” In American Society of Human Genetics, Annual Meeting, Abstracts.
APA
Van Schil, K., Naessens, S., Van De Sompele, S., Gruartmoner Roura, N., Carron, M., Dannhausen, K., De Jaegere, S., et al. (2017). Leveraging consanguinity in inherited retinal diseases uncovers missing genetic variation : rare novel disease genes and a multitude of novel variants in known disease genes. American Society of Human Genetics, Annual meeting, Abstracts. Presented at the 2017 Annual meeting of the American Society of Human Genetics (ASHG 2017).
Vancouver
1.
Van Schil K, Naessens S, Van De Sompele S, Gruartmoner Roura N, Carron M, Dannhausen K, et al. Leveraging consanguinity in inherited retinal diseases uncovers missing genetic variation : rare novel disease genes and a multitude of novel variants in known disease genes. American Society of Human Genetics, Annual meeting, Abstracts. 2017.
MLA
Van Schil, Kristof, Sarah Naessens, Stijn Van De Sompele, et al. “Leveraging Consanguinity in Inherited Retinal Diseases Uncovers Missing Genetic Variation : Rare Novel Disease Genes and a Multitude of Novel Variants in Known Disease Genes.” American Society of Human Genetics, Annual Meeting, Abstracts. 2017. Print.