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Coding and non-coding copy number variations explaining unsolved retinal dystrophies : role of genomic architectural features and underlying mechanisms

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Chicago
Van Schil, Kristof, Sarah Naessens, Stijn Van De Sompele, Miriam Bauwens, Hannah Verdin, Caroline Van Cauwenbergh, Anja Kathrin Mayer, Susanne Kohl, Bart Leroy, and Elfride De Baere. 2016. “Coding and Non-coding Copy Number Variations Explaining Unsolved Retinal Dystrophies : Role of Genomic Architectural Features and Underlying Mechanisms.” In Belgian Society of Human Genetics (BeSHG) and the Nederlandse Vereniging Voor Humane Genetica (NVHG), 1st Joint Meeting, Abstract Book.
APA
Van Schil, K., Naessens, S., Van De Sompele, S., Bauwens, M., Verdin, H., Van Cauwenbergh, C., Mayer, A. K., et al. (2016). Coding and non-coding copy number variations explaining unsolved retinal dystrophies : role of genomic architectural features and underlying mechanisms. Belgian Society of Human Genetics (BeSHG) and the Nederlandse Vereniging voor Humane Genetica (NVHG), 1st Joint meeting, Abstract book. Presented at the 1st Joint meeting of the Belgian Society of Human Genetics (BeSHG) and the Nederlandse Vereniging voor Humane Genetica (NVHG): Genetics and society.
Vancouver
1.
Van Schil K, Naessens S, Van De Sompele S, Bauwens M, Verdin H, Van Cauwenbergh C, et al. Coding and non-coding copy number variations explaining unsolved retinal dystrophies : role of genomic architectural features and underlying mechanisms. Belgian Society of Human Genetics (BeSHG) and the Nederlandse Vereniging voor Humane Genetica (NVHG), 1st Joint meeting, Abstract book. 2016.
MLA
Van Schil, Kristof, Sarah Naessens, Stijn Van De Sompele, et al. “Coding and Non-coding Copy Number Variations Explaining Unsolved Retinal Dystrophies : Role of Genomic Architectural Features and Underlying Mechanisms.” Belgian Society of Human Genetics (BeSHG) and the Nederlandse Vereniging Voor Humane Genetica (NVHG), 1st Joint Meeting, Abstract Book. 2016. Print.
@inproceedings{8555679,
  author       = {Van Schil, Kristof and Naessens, Sarah and Van De Sompele, Stijn and Bauwens, Miriam and Verdin, Hannah and Van Cauwenbergh, Caroline and Mayer, Anja Kathrin and Kohl, Susanne and Leroy, Bart and De Baere, Elfride},
  booktitle    = {Belgian Society of Human Genetics (BeSHG) and the Nederlandse Vereniging voor Humane Genetica (NVHG), 1st Joint meeting, Abstract book},
  language     = {eng},
  location     = {Leuven, Belgium},
  title        = {Coding and non-coding copy number variations explaining unsolved retinal dystrophies : role of genomic architectural features and underlying mechanisms},
  year         = {2016},
}