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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

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Chicago
Van Schil, Kristof, Sarah Naessens, Stijn Van De Sompele, Nuria Gruartmoner Roura, Marjolein Carron, Katharina Dannhausen, Sarah De Jaegere, et al. 2018. “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 Belgian Society for Human Genetics, 18th 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. (2018). Leveraging consanguinity in inherited retinal diseases uncovers missing genetic variation : rare novel disease genes and a multitude of novel variants in known disease genes. Belgian Society for Human Genetics, 18th Annual meeting, Abstracts. Presented at the 18th Annual BeSHG meeting: The epigenome in development and disease.
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. Belgian Society for Human Genetics, 18th Annual meeting, Abstracts. 2018.
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.” Belgian Society for Human Genetics, 18th Annual Meeting, Abstracts. 2018. Print.
@inproceedings{8555661,
  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    = {Belgian Society for Human Genetics, 18th Annual meeting, Abstracts},
  language     = {eng},
  location     = {Ghent, Belgium},
  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         = {2018},
}