Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience
- Author
- Karen Buysse (UGent) , BARBARA DELLE CHIAIE (UGent) , Rudy Van Coster (UGent) , Bart Loeys (UGent) , Anne De Paepe (UGent) , Geert Mortier (UGent) , Franki Speleman (UGent) and Björn Menten (UGent)
- Organization
- Keywords
- COMPARATIVE GENOMIC HYBRIDIZATION, Guidelines, Mental retardation, Copy number variation, Molecular karyotyping, Array CGH, CONSTITUTIONAL GENETIC DIAGNOSIS, COPY NUMBER VARIATION, MENTAL-RETARDATION, ARRAY-CGH, MICRODELETION SYNDROME, CONGENITAL-ANOMALIES, STRUCTURAL VARIATION, DELETION, MICROARRAYS
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Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-812683
- MLA
- Buysse, Karen, et al. “Challenges for CNV Interpretation in Clinical Molecular Karyotyping: Lessons Learned from a 1001 Sample Experience.” EUROPEAN JOURNAL OF MEDICAL GENETICS, vol. 52, no. 6, 2009, pp. 398–403, doi:10.1016/j.ejmg.2009.09.002.
- APA
- Buysse, K., DELLE CHIAIE, B., Van Coster, R., Loeys, B., De Paepe, A., Mortier, G., … Menten, B. (2009). Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience. EUROPEAN JOURNAL OF MEDICAL GENETICS, 52(6), 398–403. https://doi.org/10.1016/j.ejmg.2009.09.002
- Chicago author-date
- Buysse, Karen, BARBARA DELLE CHIAIE, Rudy Van Coster, Bart Loeys, Anne De Paepe, Geert Mortier, Franki Speleman, and Björn Menten. 2009. “Challenges for CNV Interpretation in Clinical Molecular Karyotyping: Lessons Learned from a 1001 Sample Experience.” EUROPEAN JOURNAL OF MEDICAL GENETICS 52 (6): 398–403. https://doi.org/10.1016/j.ejmg.2009.09.002.
- Chicago author-date (all authors)
- Buysse, Karen, BARBARA DELLE CHIAIE, Rudy Van Coster, Bart Loeys, Anne De Paepe, Geert Mortier, Franki Speleman, and Björn Menten. 2009. “Challenges for CNV Interpretation in Clinical Molecular Karyotyping: Lessons Learned from a 1001 Sample Experience.” EUROPEAN JOURNAL OF MEDICAL GENETICS 52 (6): 398–403. doi:10.1016/j.ejmg.2009.09.002.
- Vancouver
- 1.Buysse K, DELLE CHIAIE B, Van Coster R, Loeys B, De Paepe A, Mortier G, et al. Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience. EUROPEAN JOURNAL OF MEDICAL GENETICS. 2009;52(6):398–403.
- IEEE
- [1]K. Buysse et al., “Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience,” EUROPEAN JOURNAL OF MEDICAL GENETICS, vol. 52, no. 6, pp. 398–403, 2009.
@article{812683, author = {{Buysse, Karen and DELLE CHIAIE, BARBARA and Van Coster, Rudy and Loeys, Bart and De Paepe, Anne and Mortier, Geert and Speleman, Franki and Menten, Björn}}, issn = {{1769-7212}}, journal = {{EUROPEAN JOURNAL OF MEDICAL GENETICS}}, keywords = {{COMPARATIVE GENOMIC HYBRIDIZATION,Guidelines,Mental retardation,Copy number variation,Molecular karyotyping,Array CGH,CONSTITUTIONAL GENETIC DIAGNOSIS,COPY NUMBER VARIATION,MENTAL-RETARDATION,ARRAY-CGH,MICRODELETION SYNDROME,CONGENITAL-ANOMALIES,STRUCTURAL VARIATION,DELETION,MICROARRAYS}}, language = {{eng}}, number = {{6}}, pages = {{398--403}}, title = {{Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience}}, url = {{http://doi.org/10.1016/j.ejmg.2009.09.002}}, volume = {{52}}, year = {{2009}}, }
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