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Identification of novel homozygous deletions in consanguineous pedigrees as a shortcut to candidate gene discovery in hereditary blindness

(2013) EUROPEAN JOURNAL OF HUMAN GENETICS. 21(suppl. 2). p.119-120
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Chicago
Van Schil, Kristof, Thomy De Ravel, Bart Leroy, Hannah Verdin, Frauke Coppieters, Françoise Meire, and Elfride De Baere. 2013. “Identification of Novel Homozygous Deletions in Consanguineous Pedigrees as a Shortcut to Candidate Gene Discovery in Hereditary Blindness.” In European Journal of Human Genetics, 21:119–120.
APA
Van Schil, K., De Ravel, T., Leroy, B., Verdin, H., Coppieters, F., Meire, F., & De Baere, E. (2013). Identification of novel homozygous deletions in consanguineous pedigrees as a shortcut to candidate gene discovery in hereditary blindness. EUROPEAN JOURNAL OF HUMAN GENETICS (Vol. 21, pp. 119–120). Presented at the European Human Genetics Conference 2013 (ESHG 2013).
Vancouver
1.
Van Schil K, De Ravel T, Leroy B, Verdin H, Coppieters F, Meire F, et al. Identification of novel homozygous deletions in consanguineous pedigrees as a shortcut to candidate gene discovery in hereditary blindness. EUROPEAN JOURNAL OF HUMAN GENETICS. 2013. p. 119–20.
MLA
Van Schil, Kristof, Thomy De Ravel, Bart Leroy, et al. “Identification of Novel Homozygous Deletions in Consanguineous Pedigrees as a Shortcut to Candidate Gene Discovery in Hereditary Blindness.” European Journal of Human Genetics. Vol. 21. 2013. 119–120. Print.
@inproceedings{8555750,
  articleno    = {abstract P03.02},
  author       = {Van Schil, Kristof and De Ravel, Thomy and Leroy, Bart and Verdin, Hannah and Coppieters, Frauke and Meire, Fran\c{c}oise and De Baere, Elfride},
  booktitle    = {EUROPEAN JOURNAL OF HUMAN GENETICS},
  issn         = {1018-4813},
  language     = {eng},
  location     = {Paris, France},
  number       = {suppl. 2},
  pages        = {abstract P03.02:119--abstract P03.02:120},
  title        = {Identification of novel homozygous deletions in consanguineous pedigrees as a shortcut to candidate gene discovery in hereditary blindness},
  url          = {https://www.eshg.org/fileadmin/www.eshg.org/conferences/2013/ESHG2013AbstractsWebsite.pdf},
  volume       = {21},
  year         = {2013},
}