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Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13).

EMR DE LEENHEER, H KUNST, WT MCGUIRT, SD PRASAD, M Brown, P HUYGEN, R SMITH and WRJ CREMERS (2001) ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY. 127(1). p.13-17
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
journal title
ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY
volume
127
issue
1
pages
13-17 pages
Web of Science type
Article
Web of Science id
000166329100001
JCR category
OTORHINOLARYNGOLOGY
JCR impact factor
1.121 (2001)
JCR rank
8/29 (2001)
JCR quartile
2 (2001)
ISSN
0886-4470
language
English
UGent publication?
yes
classification
A1
id
142895
handle
http://hdl.handle.net/1854/LU-142895
date created
2004-01-14 13:37:00
date last changed
2016-12-19 15:38:06
@article{142895,
  author       = {DE LEENHEER, EMR and KUNST, H and MCGUIRT, WT and PRASAD, SD and Brown, M and HUYGEN, P and SMITH, R and CREMERS, WRJ},
  issn         = {0886-4470},
  journal      = {ARCHIVES OF OTOLARYNGOLOGY-HEAD \& NECK SURGERY},
  language     = {eng},
  number       = {1},
  pages        = {13--17},
  title        = {Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13).},
  volume       = {127},
  year         = {2001},
}

Chicago
DE LEENHEER, EMR, H KUNST, WT MCGUIRT, SD PRASAD, M Brown, P HUYGEN, R SMITH, and WRJ CREMERS. 2001. “Autosomal Dominant Inherited Hearing Impairment Caused by a Missense Mutation in COL11A2 (DFNA13).” Archives of Otolaryngology-head & Neck Surgery 127 (1): 13–17.
APA
DE LEENHEER, E., KUNST, H., MCGUIRT, W., PRASAD, S., Brown, M., HUYGEN, P., SMITH, R., et al. (2001). Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13). ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 127(1), 13–17.
Vancouver
1.
DE LEENHEER E, KUNST H, MCGUIRT W, PRASAD S, Brown M, HUYGEN P, et al. Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13). ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY. 2001;127(1):13–7.
MLA
DE LEENHEER, EMR, H KUNST, WT MCGUIRT, et al. “Autosomal Dominant Inherited Hearing Impairment Caused by a Missense Mutation in COL11A2 (DFNA13).” ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY 127.1 (2001): 13–17. Print.