Cite
Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing.
MLA
Goossens, Dirk, et al. “Simultaneous Mutation and Copy Number Variation (CNV) Detection by Multiplex PCR-Based GS-FLX Sequencing.” Human Mutation, vol. 30, no. 3, Mar. 2009, pp. 472–76. EBSCOhost, https://doi.org/10.1002/humu.20873.
APA
Goossens, D., Moens, L. N., Nelis, E., Lenaerts, A.-S., Glassee, W., Kalbe, A., Frey, B., Kopal, G., Jonghe, P. D., Rijk, P. D., & Del-Favero, J. (2009). Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing. Human Mutation, 30(3), 472–476. https://doi.org/10.1002/humu.20873
Chicago
Goossens, Dirk, Lotte N. Moens, Eva Nelis, An-Sofie Lenaerts, Wim Glassee, Andreas Kalbe, Bruno Frey, et al. 2009. “Simultaneous Mutation and Copy Number Variation (CNV) Detection by Multiplex PCR-Based GS-FLX Sequencing.” Human Mutation 30 (3): 472–76. doi:10.1002/humu.20873.