Advanced search
Add to list

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)
Author
Organization

Citation

Please use this url to cite or link to this publication:

MLA
Menten, Björn, 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, vol. 48, no. 3, Elsevier Science, 2005, pp. 301–09.
APA
Menten, B., 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.
Chicago author-date
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): 301–9.
Chicago author-date (all authors)
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.
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. 2005;48(3):301–9.
IEEE
[1]
B. Menten 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, vol. 48, no. 3, pp. 301–309, 2005.
@article{333252,
  author       = {{Menten, Björn 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}},
}

Web of Science
Times cited: