APA

de Ligt J., Boone P. M., Pfundt R., Vissers L. E. L. M., Richmond T., Geoghegan J., O'Moore K., de Leeuw N., Shaw C., Brunner H. G., Lupski J. R., Veltman J. A. & Hehir-Kwa J. Y. (20140721). Detection of clinically relevant copy number variants with whole-exome sequencing. : Human mutation.

Chicago

de Ligt Joep, Boone Philip M, Pfundt Rolph, Vissers Lisenka E L M, Richmond Todd, Geoghegan Joel, O'Moore Kathleen, de Leeuw Nicole, Shaw Christine, Brunner Han G, Lupski James R, Veltman Joris A and Hehir-Kwa Jayne Y. 20140721. Detection of clinically relevant copy number variants with whole-exome sequencing. : Human mutation.

Harvard

de Ligt J., Boone P. M., Pfundt R., Vissers L. E. L. M., Richmond T., Geoghegan J., O'Moore K., de Leeuw N., Shaw C., Brunner H. G., Lupski J. R., Veltman J. A. and Hehir-Kwa J. Y. (20140721). Detection of clinically relevant copy number variants with whole-exome sequencing. : Human mutation.

MLA

de Ligt Joep, Boone Philip M, Pfundt Rolph, Vissers Lisenka E L M, Richmond Todd, Geoghegan Joel, O'Moore Kathleen, de Leeuw Nicole, Shaw Christine, Brunner Han G, Lupski James R, Veltman Joris A and Hehir-Kwa Jayne Y. Detection of clinically relevant copy number variants with whole-exome sequencing. : Human mutation. 20140721.