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Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type

Björn Menten UGent, Karen Buysse UGent, Jo Vandesompele UGent, Els De Smet UGent, Anne De Paepe UGent, Franki Speleman UGent and Geert Mortier UGent (2005) EUROPEAN JOURNAL OF MEDICAL GENETICS. 48(3). p.301-309
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle
publication status
published
subject
journal title
EUROPEAN JOURNAL OF MEDICAL GENETICS
Eur. J. Med. Genet.
volume
48
issue
3
pages
301-309 pages
publisher
Elsevier Science
Web of Science type
Article
Web of Science id
000232614200009
JCR category
GENETICS & HEREDITY
JCR rank
120 (2005)
JCR quartile
4 (2005)
ISSN
1769-7212
language
English
UGent publication?
yes
classification
A1
id
333252
handle
http://hdl.handle.net/1854/LU-333252
date created
2006-04-27 11:16:00
date last changed
2015-06-17 10:34:30
@article{333252,
  author       = {Menten, Bj{\"o}rn and Buysse, Karen and Vandesompele, Jo and De Smet, Els and De Paepe, Anne and Speleman, Franki and Mortier, Geert},
  issn         = {1769-7212},
  journal      = {EUROPEAN JOURNAL OF MEDICAL GENETICS},
  language     = {eng},
  number       = {3},
  pages        = {301--309},
  publisher    = {Elsevier Science},
  title        = {Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type},
  volume       = {48},
  year         = {2005},
}

Chicago
Menten, Björn, Karen Buysse, Jo Vandesompele, Els De Smet, Anne De Paepe, Franki Speleman, and Geert Mortier. 2005. “Identification of an Unbalanced X-autosome Translocation by Array CGH in a Boy with a Syndromic Form of Chondrodysplasia Punctata Brachytelephalangic Type.” European Journal of Medical Genetics 48 (3): 301–309.
APA
Menten, Björn, Buysse, K., Vandesompele, J., De Smet, E., De Paepe, A., Speleman, F., & Mortier, G. (2005). Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type. EUROPEAN JOURNAL OF MEDICAL GENETICS, 48(3), 301–309.
Vancouver
1.
Menten B, Buysse K, Vandesompele J, De Smet E, De Paepe A, Speleman F, et al. Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type. EUROPEAN JOURNAL OF MEDICAL GENETICS. Elsevier Science; 2005;48(3):301–9.
MLA
Menten, Björn, Karen Buysse, Jo Vandesompele, et al. “Identification of an Unbalanced X-autosome Translocation by Array CGH in a Boy with a Syndromic Form of Chondrodysplasia Punctata Brachytelephalangic Type.” EUROPEAN JOURNAL OF MEDICAL GENETICS 48.3 (2005): 301–309. Print.