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Clinical and radiographic features of a family with hypochondroplasia owing to a novel Asn540Ser mutation in the fibroblast growth factor receptor 3 gene

Geert Mortier UGent, Lieve Nuytinck UGent, Margarita Craen UGent, Jean-Pierre Renard, Juliaan Leroy UGent and Anne De Paepe UGent (2000) JOURNAL OF MEDICAL GENETICS. 37(3). p.220-224
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (letterNote)
publication status
published
subject
journal title
JOURNAL OF MEDICAL GENETICS
J. Med. Genet.
volume
37
issue
3
pages
220-224 pages
Web of Science type
Letter
Web of Science id
000085797500013
ISSN
0022-2593
DOI
10.1136/jmg.37.3.220
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
170793
handle
http://hdl.handle.net/1854/LU-170793
date created
2004-01-14 13:40:00
date last changed
2015-06-17 09:48:00
@article{170793,
  author       = {Mortier, Geert and Nuytinck, Lieve and Craen, Margarita and Renard, Jean-Pierre and Leroy, Juliaan and De Paepe, Anne},
  issn         = {0022-2593},
  journal      = {JOURNAL OF MEDICAL GENETICS},
  language     = {eng},
  number       = {3},
  pages        = {220--224},
  title        = {Clinical and radiographic features of a family with hypochondroplasia owing to a novel Asn540Ser mutation in the fibroblast growth factor receptor 3 gene},
  url          = {http://dx.doi.org/10.1136/jmg.37.3.220},
  volume       = {37},
  year         = {2000},
}

Chicago
Mortier, Geert, Lieve Nuytinck, Margarita Craen, Jean-Pierre Renard, Juliaan Leroy, and Anne De Paepe. 2000. “Clinical and Radiographic Features of a Family with Hypochondroplasia Owing to a Novel Asn540Ser Mutation in the Fibroblast Growth Factor Receptor 3 Gene.” Journal of Medical Genetics 37 (3): 220–224.
APA
Mortier, Geert, Nuytinck, L., Craen, M., Renard, J.-P., Leroy, J., & De Paepe, A. (2000). Clinical and radiographic features of a family with hypochondroplasia owing to a novel Asn540Ser mutation in the fibroblast growth factor receptor 3 gene. JOURNAL OF MEDICAL GENETICS, 37(3), 220–224.
Vancouver
1.
Mortier G, Nuytinck L, Craen M, Renard J-P, Leroy J, De Paepe A. Clinical and radiographic features of a family with hypochondroplasia owing to a novel Asn540Ser mutation in the fibroblast growth factor receptor 3 gene. JOURNAL OF MEDICAL GENETICS. 2000;37(3):220–4.
MLA
Mortier, Geert, Lieve Nuytinck, Margarita Craen, et al. “Clinical and Radiographic Features of a Family with Hypochondroplasia Owing to a Novel Asn540Ser Mutation in the Fibroblast Growth Factor Receptor 3 Gene.” JOURNAL OF MEDICAL GENETICS 37.3 (2000): 220–224. Print.