Identification of novel homozygous deletions in consanguineous pedigrees as a shortcut to candidate gene discovery in retinal dystrophies
- Author
- Kristof Van Schil (UGent) , Françoise Meire, Thomy De Ravel, Bart Leroy (UGent) , Hannah Verdin (UGent) , Frauke Coppieters (UGent) and Elfride De Baere (UGent)
- Organization
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-8555752
- MLA
- Van Schil, Kristof, et al. “Identification of Novel Homozygous Deletions in Consanguineous Pedigrees as a Shortcut to Candidate Gene Discovery in Retinal Dystrophies.” Belgian Society of Human Genetics, 13th Annual Meeting, Abstracts, 2013.
- APA
- Van Schil, K., Meire, F., De Ravel, T., Leroy, B., Verdin, H., Coppieters, F., & De Baere, E. (2013). Identification of novel homozygous deletions in consanguineous pedigrees as a shortcut to candidate gene discovery in retinal dystrophies. Belgian Society of Human Genetics, 13th Annual Meeting, Abstracts. Presented at the 13th Annual meeting of the Belgian Society of Human Genetics (BeSHG) : Genetics of human development EXPOsed, Brussels, Belgium.
- Chicago author-date
- Van Schil, Kristof, Françoise Meire, Thomy De Ravel, Bart Leroy, Hannah Verdin, Frauke Coppieters, and Elfride De Baere. 2013. “Identification of Novel Homozygous Deletions in Consanguineous Pedigrees as a Shortcut to Candidate Gene Discovery in Retinal Dystrophies.” In Belgian Society of Human Genetics, 13th Annual Meeting, Abstracts.
- Chicago author-date (all authors)
- Van Schil, Kristof, Françoise Meire, Thomy De Ravel, Bart Leroy, Hannah Verdin, Frauke Coppieters, and Elfride De Baere. 2013. “Identification of Novel Homozygous Deletions in Consanguineous Pedigrees as a Shortcut to Candidate Gene Discovery in Retinal Dystrophies.” In Belgian Society of Human Genetics, 13th Annual Meeting, Abstracts.
- Vancouver
- 1.Van Schil K, Meire F, De Ravel T, Leroy B, Verdin H, Coppieters F, et al. Identification of novel homozygous deletions in consanguineous pedigrees as a shortcut to candidate gene discovery in retinal dystrophies. In: Belgian Society of Human Genetics, 13th Annual meeting, Abstracts. 2013.
- IEEE
- [1]K. Van Schil et al., “Identification of novel homozygous deletions in consanguineous pedigrees as a shortcut to candidate gene discovery in retinal dystrophies,” in Belgian Society of Human Genetics, 13th Annual meeting, Abstracts, Brussels, Belgium, 2013.
@inproceedings{8555752, author = {{Van Schil, Kristof and Meire, Françoise and De Ravel, Thomy and Leroy, Bart and Verdin, Hannah and Coppieters, Frauke and De Baere, Elfride}}, booktitle = {{Belgian Society of Human Genetics, 13th Annual meeting, Abstracts}}, language = {{eng}}, location = {{Brussels, Belgium}}, title = {{Identification of novel homozygous deletions in consanguineous pedigrees as a shortcut to candidate gene discovery in retinal dystrophies}}, year = {{2013}}, }