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Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1]

Mine Arslan-Kirchner, Eloisa Arbustini, Catherine Boileau, Anne Child, Gwenaelle Collod-Beroud, Anne De Paepe UGent, Jörg Epplen, Guillaume Jondeau, Bart Loeys UGent and Laurence Faivre (2010) EUROPEAN JOURNAL OF HUMAN GENETICS. 18(9).
Please use this url to cite or link to this publication:
author
organization
year
type
misc (editorialMaterial)
publication status
published
subject
keyword
DISORDERS, RECURRENCE, TGFBR2 MUTATIONS, I FIBRILLINOPATHIES, DIAGNOSTIC-CRITERIA, MOSAICISM, 1009 PROBANDS, FEATURES, ECTOPIA LENTIS, IDENTIFICATION
in
EUROPEAN JOURNAL OF HUMAN GENETICS
Eur. J. Hum. Genet.
volume
18
issue
9
pages
4 pages
Web of Science type
Editorial Material
Web of Science id
000281117400024
JCR category
GENETICS & HEREDITY
JCR impact factor
4.38 (2010)
JCR rank
30/154 (2010)
JCR quartile
1 (2010)
ISSN
1018-4813
DOI
10.1038/ejhg.2010.42
language
English
UGent publication?
yes
classification
V
copyright statement
I have transferred the copyright for this publication to the publisher
id
1064550
handle
http://hdl.handle.net/1854/LU-1064550
date created
2010-10-26 15:15:05
date last changed
2017-04-07 08:42:14
@misc{1064550,
  author       = {Arslan-Kirchner, Mine and Arbustini, Eloisa and Boileau, Catherine and Child, Anne and Collod-Beroud, Gwenaelle and De Paepe, Anne and Epplen, J{\"o}rg and Jondeau, Guillaume and Loeys, Bart and Faivre, Laurence},
  issn         = {1018-4813},
  keyword      = {DISORDERS,RECURRENCE,TGFBR2 MUTATIONS,I FIBRILLINOPATHIES,DIAGNOSTIC-CRITERIA,MOSAICISM,1009 PROBANDS,FEATURES,ECTOPIA LENTIS,IDENTIFICATION},
  language     = {eng},
  number       = {9},
  pages        = {4},
  series       = {EUROPEAN JOURNAL OF HUMAN GENETICS},
  title        = {Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1]},
  url          = {http://dx.doi.org/10.1038/ejhg.2010.42},
  volume       = {18},
  year         = {2010},
}

Chicago
Arslan-Kirchner, Mine, Eloisa Arbustini, Catherine Boileau, Anne Child, Gwenaelle Collod-Beroud, Anne De Paepe, Jörg Epplen, Guillaume Jondeau, Bart Loeys, and Laurence Faivre. 2010. “Clinical Utility Gene Card for: Marfan Syndrome Type 1 and Related Phenotypes [FBN1].” European Journal of Human Genetics.
APA
Arslan-Kirchner, M., Arbustini, E., Boileau, C., Child, A., Collod-Beroud, G., De Paepe, A., Epplen, J., et al. (2010). Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1]. EUROPEAN JOURNAL OF HUMAN GENETICS.
Vancouver
1.
Arslan-Kirchner M, Arbustini E, Boileau C, Child A, Collod-Beroud G, De Paepe A, et al. Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1]. EUROPEAN JOURNAL OF HUMAN GENETICS. 2010.
MLA
Arslan-Kirchner, Mine, Eloisa Arbustini, Catherine Boileau, et al. “Clinical Utility Gene Card for: Marfan Syndrome Type 1 and Related Phenotypes [FBN1].” EUROPEAN JOURNAL OF HUMAN GENETICS 2010 : n. pag. Print.