Ghent University Academic Bibliography

Advanced

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

Kristof Van Schil UGent, Thomy De Ravel, Bart Leroy UGent, Hannah Verdin UGent, Frauke Coppieters, Françoise Meire and Elfride De Baere UGent (2013) EUROPEAN JOURNAL OF HUMAN GENETICS. 21(suppl. 2). p.119-120
Please use this url to cite or link to this publication:
author
organization
alternative title
Identification of novel homozygous deletions in consanguineous pedigrees as a shortcut to candidate gene discovery in retinal dystrophies
year
type
conference (poster)
publication status
published
subject
in
EUROPEAN JOURNAL OF HUMAN GENETICS
Eur. J. Hum. Genet.
volume
21
issue
suppl. 2
article number
abstract P03.02
pages
119 - 120
conference name
European Human Genetics Conference 2013 (ESHG 2013)
conference location
Paris, France
conference start
2013-06-08
conference end
2013-06-11
JCR category
GENETICS & HEREDITY
JCR impact factor
4.225 (2013)
JCR rank
38/165 (2013)
JCR quartile
1 (2013)
ISSN
1018-4813
language
English
UGent publication?
yes
classification
C3
id
8555750
handle
http://hdl.handle.net/1854/LU-8555750
alternative location
https://www.eshg.org/fileadmin/www.eshg.org/conferences/2013/ESHG2013AbstractsWebsite.pdf
date created
2018-03-15 07:11:48
date last changed
2018-05-17 07:30:47
@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},
}

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.