APA
Pfundt R., Del Rosario M., Vissers L. E. L. M., Kwint M. P., Janssen I. M., de Leeuw N., Yntema H. G., Nelen M. R., Lugtenberg D., Kamsteeg E., Wieskamp N., Stegmann A. P. A., Stevens S. J. C., Rodenburg R. J. T., Simons A., Mensenkamp A. R., Rinne T., Gilissen C., Scheffer H., Veltman J. A. & Hehir-Kwa J. Y. (20180213). Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders. : Genetics in medicine : official journal of the American College of Medical Genetics.
Chicago
Pfundt Rolph, Del Rosario Marisol, Vissers Lisenka E L M, Kwint Michael P, Janssen Irene M, de Leeuw Nicole, Yntema Helger G, Nelen Marcel R, Lugtenberg Dorien, Kamsteeg Erik-Jan, Wieskamp Nienke, Stegmann Alexander P A, Stevens Servi J C, Rodenburg Richard J T, Simons Annet, Mensenkamp Arjen R, Rinne Tuula, Gilissen Christian, Scheffer Hans, Veltman Joris A and Hehir-Kwa Jayne Y. 20180213. Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders. : Genetics in medicine : official journal of the American College of Medical Genetics.
Harvard
Pfundt R., Del Rosario M., Vissers L. E. L. M., Kwint M. P., Janssen I. M., de Leeuw N., Yntema H. G., Nelen M. R., Lugtenberg D., Kamsteeg E., Wieskamp N., Stegmann A. P. A., Stevens S. J. C., Rodenburg R. J. T., Simons A., Mensenkamp A. R., Rinne T., Gilissen C., Scheffer H., Veltman J. A. and Hehir-Kwa J. Y. (20180213). Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders. : Genetics in medicine : official journal of the American College of Medical Genetics.
MLA
Pfundt Rolph, Del Rosario Marisol, Vissers Lisenka E L M, Kwint Michael P, Janssen Irene M, de Leeuw Nicole, Yntema Helger G, Nelen Marcel R, Lugtenberg Dorien, Kamsteeg Erik-Jan, Wieskamp Nienke, Stegmann Alexander P A, Stevens Servi J C, Rodenburg Richard J T, Simons Annet, Mensenkamp Arjen R, Rinne Tuula, Gilissen Christian, Scheffer Hans, Veltman Joris A and Hehir-Kwa Jayne Y. Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders. : Genetics in medicine : official journal of the American College of Medical Genetics. 20180213.