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Exome-based RetNet panel analysis in a Belgian cohort with inherited retinal disease (IRD) expands the molecular and phenotypic spectrum of recently identified IRD genes

Stijn Van De Sompele UGent, Kristof Van Schil UGent, Caroline Van Cauwenbergh UGent, Toon Rosseel UGent, Sarah De Jaegere, Thalia Van Laethem UGent, Irina Balikova, Bart Leroy UGent, Frauke Coppieters and Elfride De Baere UGent (2018) European Human Genetics conference, Abstracts.
Please use this url to cite or link to this publication:
author
organization
year
type
conference (meetingAbstract)
publication status
published
subject
in
European Human Genetics conference, Abstracts
conference name
European Human Genetics conference 2018 (ESHG 2018)
conference organizer
European Society of Human Genetics (ESHG)
conference location
Milan, Italy
conference start
2018-06-16
conference end
2018-06-19
language
English
UGent publication?
yes
classification
C3
id
8556229
handle
http://hdl.handle.net/1854/LU-8556229
date created
2018-03-16 12:38:29
date last changed
2018-05-17 08:29:44
@inproceedings{8556229,
  author       = {Van De Sompele, Stijn and Van Schil, Kristof and Van Cauwenbergh, Caroline and Rosseel, Toon and De Jaegere, Sarah and Van Laethem, Thalia and Balikova, Irina and Leroy, Bart and Coppieters, Frauke and De Baere, Elfride},
  booktitle    = {European Human Genetics conference, Abstracts},
  language     = {eng},
  location     = {Milan, Italy},
  title        = {Exome-based RetNet panel analysis in a Belgian cohort with inherited retinal disease (IRD) expands the molecular and phenotypic spectrum of recently identified IRD genes},
  year         = {2018},
}

Chicago
Van De Sompele, Stijn, Kristof Van Schil, Caroline Van Cauwenbergh, Toon Rosseel, Sarah De Jaegere, Thalia Van Laethem, Irina Balikova, Bart Leroy, Frauke Coppieters, and Elfride De Baere. 2018. “Exome-based RetNet Panel Analysis in a Belgian Cohort with Inherited Retinal Disease (IRD) Expands the Molecular and Phenotypic Spectrum of Recently Identified IRD Genes.” In European Human Genetics Conference, Abstracts.
APA
Van De Sompele, S., Van Schil, K., Van Cauwenbergh, C., Rosseel, T., De Jaegere, S., Van Laethem, T., Balikova, I., et al. (2018). Exome-based RetNet panel analysis in a Belgian cohort with inherited retinal disease (IRD) expands the molecular and phenotypic spectrum of recently identified IRD genes. European Human Genetics conference, Abstracts. Presented at the European Human Genetics conference 2018 (ESHG 2018).
Vancouver
1.
Van De Sompele S, Van Schil K, Van Cauwenbergh C, Rosseel T, De Jaegere S, Van Laethem T, et al. Exome-based RetNet panel analysis in a Belgian cohort with inherited retinal disease (IRD) expands the molecular and phenotypic spectrum of recently identified IRD genes. European Human Genetics conference, Abstracts. 2018.
MLA
Van De Sompele, Stijn, Kristof Van Schil, Caroline Van Cauwenbergh, et al. “Exome-based RetNet Panel Analysis in a Belgian Cohort with Inherited Retinal Disease (IRD) Expands the Molecular and Phenotypic Spectrum of Recently Identified IRD Genes.” European Human Genetics Conference, Abstracts. 2018. Print.