Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type
- Author
- Björn Menten (UGent) , Karen Buysse (UGent) , Jo Vandesompele (UGent) , Els De Smet (UGent) , Anne De Paepe (UGent) , Franki Speleman (UGent) and Geert Mortier (UGent)
- Organization
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-333252
- 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}}, }