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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 (UGent) , Thalia Van Laethem (UGent) , Irina Balikova (UGent) , Bart Leroy (UGent) , Frauke Coppieters (UGent) and Elfride De Baere (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 (IRD) Expands the Molecular and Phenotypic Spectrum of Recently Identified IRD Genes.” EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, no. 1, 2019, pp. 54–54.
APA
Van De Sompele, S., Van Schil, K., Van Cauwenbergh, C., Rosseel, T., De Jaegere, S., Van Laethem, T., … De Baere, E. (2019). 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 JOURNAL OF HUMAN GENETICS (Vol. 27, pp. 54–54). Milan, Italy.
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, Frauke Coppieters, and Elfride De Baere. 2019. “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 JOURNAL OF HUMAN GENETICS, 27:54–54.
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, Frauke Coppieters, and Elfride De Baere. 2019. “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 JOURNAL OF HUMAN GENETICS, 27:54–54.
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. In: EUROPEAN JOURNAL OF HUMAN GENETICS. 2019. p. 54–54.
IEEE
[1]
S. Van De Sompele 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,” in EUROPEAN JOURNAL OF HUMAN GENETICS, Milan, Italy, 2019, vol. 27, no. 1, pp. 54–54.
@inproceedings{8556229,
  articleno    = {P02.25D},
  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 JOURNAL OF HUMAN GENETICS},
  issn         = {1018-4813},
  language     = {eng},
  location     = {Milan, Italy},
  number       = {1},
  pages        = {P02.25D:54--P02.25D:54},
  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},
  volume       = {27},
  year         = {2019},
}

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