Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly
(2004) JOURNAL OF MEDICAL GENETICS. 41(1). p.60-67
Please use this url to cite or link to this publication:
http://hdl.handle.net/1854/LU-348799
- author
- RR RICHARDSON, D DONNAI, Françoise Meire UGent and MJ DIXON
- organization
- year
- 2004
- type
- journalArticle (original)
- publication status
- published
- subject
- journal title
- JOURNAL OF MEDICAL GENETICS
- J. Med. Genet.
- volume
- 41
- issue
- 1
- pages
- 60-67 pages
- publisher
- B M J PUBLISHING GROUP
- Web of Science type
- Article
- Web of Science id
- 000188217600015
- ISSN
- 1468-6244
- language
- English
- UGent publication?
- yes
- classification
- A1
- id
- 348799
- handle
- http://hdl.handle.net/1854/LU-348799
- date created
- 2005-06-17 09:00:00
- date last changed
- 2016-12-19 15:44:02
@article{348799,
author = {RICHARDSON, RR and DONNAI, D and Meire, Fran\c{c}oise and DIXON, MJ},
issn = {1468-6244},
journal = {JOURNAL OF MEDICAL GENETICS},
language = {eng},
number = {1},
pages = {60--67},
publisher = {B M J PUBLISHING GROUP},
title = {Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly},
volume = {41},
year = {2004},
}
- Chicago
- RICHARDSON, RR, D DONNAI, Françoise Meire, and MJ DIXON. 2004. “Expression of Gja1 Correlates with the Phenotype Observed in Oculodentodigital Syndrome/type III Syndactyly.” Journal of Medical Genetics 41 (1): 60–67.
- APA
- RICHARDSON, R., DONNAI, D., Meire, F., & DIXON, M. (2004). Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly. JOURNAL OF MEDICAL GENETICS, 41(1), 60–67.
- Vancouver
- 1.RICHARDSON R, DONNAI D, Meire F, DIXON M. Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly. JOURNAL OF MEDICAL GENETICS. B M J PUBLISHING GROUP; 2004;41(1):60–7.
- MLA
- RICHARDSON, RR, D DONNAI, Françoise Meire, et al. “Expression of Gja1 Correlates with the Phenotype Observed in Oculodentodigital Syndrome/type III Syndactyly.” JOURNAL OF MEDICAL GENETICS 41.1 (2004): 60–67. Print.