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Exome-based RetNet panel analysis in a Belgian cohort with inherited retinal disease 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 (UGent) , Thalia Van Laethem (UGent) , Irina Balikova (UGent) , Bart Leroy (UGent) , Elfride De Baere (UGent) and Frauke Coppieters (UGent)
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MLA
Van de Sompele, Stijn, et al. “Exome-Based RetNet Panel Analysis in a Belgian Cohort with Inherited Retinal Disease Expands the Molecular and Phenotypic Spectrum of Recently Identified IRD Genes.” Belgian Society for Human Genetics, 18th Annual Meeting, Abstracts, 2018.
APA
Van de Sompele, S., Van Schil, K., Van Cauwenbergh, C., Rosseel, T., De Jaegere, S., Van Laethem, T., … Coppieters, F. (2018). Exome-based RetNet panel analysis in a Belgian cohort with inherited retinal disease expands the molecular and phenotypic spectrum of recently identified iRD genes. Belgian Society for Human Genetics, 18th Annual Meeting, Abstracts. Presented at the 18th Annual BeSHG meeting: The epigenome in development and disease, Ghent, Belgium.
Chicago author-date
Van de Sompele, Stijn, Kristof Van Schil, Caroline Van Cauwenbergh, Toon Rosseel, Sarah De Jaegere, Thalia Van Laethem, Irina Balikova, Bart Leroy, Elfride De Baere, and Frauke Coppieters. 2018. “Exome-Based RetNet Panel Analysis in a Belgian Cohort with Inherited Retinal Disease Expands the Molecular and Phenotypic Spectrum of Recently Identified IRD Genes.” In Belgian Society for Human Genetics, 18th Annual Meeting, Abstracts.
Chicago author-date (all authors)
Van de Sompele, Stijn, Kristof Van Schil, Caroline Van Cauwenbergh, Toon Rosseel, Sarah De Jaegere, Thalia Van Laethem, Irina Balikova, Bart Leroy, Elfride De Baere, and Frauke Coppieters. 2018. “Exome-Based RetNet Panel Analysis in a Belgian Cohort with Inherited Retinal Disease Expands the Molecular and Phenotypic Spectrum of Recently Identified IRD Genes.” In Belgian Society for Human Genetics, 18th Annual Meeting, Abstracts.
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 expands the molecular and phenotypic spectrum of recently identified iRD genes. In: Belgian Society for Human Genetics, 18th Annual meeting, Abstracts. 2018.
IEEE
[1]
S. Van de Sompele et al., “Exome-based RetNet panel analysis in a Belgian cohort with inherited retinal disease expands the molecular and phenotypic spectrum of recently identified iRD genes,” in Belgian Society for Human Genetics, 18th Annual meeting, Abstracts, Ghent, Belgium, 2018.
@inproceedings{8556179,
  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 De Baere, Elfride and Coppieters, Frauke}},
  booktitle    = {{Belgian Society for Human Genetics, 18th Annual meeting, Abstracts}},
  language     = {{eng}},
  location     = {{Ghent, Belgium}},
  title        = {{Exome-based RetNet panel analysis in a Belgian cohort with inherited retinal disease expands the molecular and phenotypic spectrum of recently identified iRD genes}},
  year         = {{2018}},
}