APA
Heinzen E. L., Radtke R. A., Urban T. J., Cavalleri G. L., Depondt C., Need A. C., Walley N. M., Nicoletti P., Ge D., Catarino C. B., Duncan J. S., Kasperaviciūte D., Tate S. K., Caboclo L. O., Sander J. W., Clayton L., Linney K. N., Shianna K. V., Gumbs C. E., Smith J., Cronin K. D., Maia J. M., Doherty C. P., Pandolfo M., Leppert D., Middleton L. T., Gibson R. A., Johnson M. R., Matthews P. M., Hosford D., Kälviäinen R., Eriksson K., Kantanen A., Dorn T., Hansen J., Krämer G., Steinhoff B. J., Wieser H., Zumsteg D., Ortega M., Wood N. W., Huxley-Jones J., Mikati M., Gallentine W. B., Husain A. M., Buckley P. G., Stallings R. L., Podgoreanu M. V., Delanty N., Sisodiya S. M. & Goldstein D. B. (20100621). Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes. : American journal of human genetics.
Chicago
Heinzen Erin L, Radtke Rodney A, Urban Thomas J, Cavalleri Gianpiero L, Depondt Chantal, Need Anna C, Walley Nicole M, Nicoletti Paola, Ge Dongliang, Catarino Claudia B, Duncan John S, Kasperaviciūte Dalia, Tate Sarah K, Caboclo Luis O, Sander Josemir W, Clayton Lisa, Linney Kristen N, Shianna Kevin V, Gumbs Curtis E, Smith Jason, Cronin Kenneth D, Maia Jessica M, Doherty Colin P, Pandolfo Massimo, Leppert David, Middleton Lefkos T, Gibson Rachel A, Johnson Michael R, Matthews Paul M, Hosford David, Kälviäinen Reetta, Eriksson Kai, Kantanen Anne-Mari, Dorn Thomas, Hansen Jörg, Krämer Günter, Steinhoff Bernhard J, Wieser Heinz-Gregor, Zumsteg Dominik, Ortega Marcos, Wood Nicholas W, Huxley-Jones Julie, Mikati Mohamad, Gallentine William B, Husain Aatif M, Buckley Patrick G, Stallings Ray L, Podgoreanu Mihai V, Delanty Norman, Sisodiya Sanjay M and Goldstein David B. 20100621. Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes. : American journal of human genetics.
Harvard
Heinzen E. L., Radtke R. A., Urban T. J., Cavalleri G. L., Depondt C., Need A. C., Walley N. M., Nicoletti P., Ge D., Catarino C. B., Duncan J. S., Kasperaviciūte D., Tate S. K., Caboclo L. O., Sander J. W., Clayton L., Linney K. N., Shianna K. V., Gumbs C. E., Smith J., Cronin K. D., Maia J. M., Doherty C. P., Pandolfo M., Leppert D., Middleton L. T., Gibson R. A., Johnson M. R., Matthews P. M., Hosford D., Kälviäinen R., Eriksson K., Kantanen A., Dorn T., Hansen J., Krämer G., Steinhoff B. J., Wieser H., Zumsteg D., Ortega M., Wood N. W., Huxley-Jones J., Mikati M., Gallentine W. B., Husain A. M., Buckley P. G., Stallings R. L., Podgoreanu M. V., Delanty N., Sisodiya S. M. and Goldstein D. B. (20100621). Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes. : American journal of human genetics.
MLA
Heinzen Erin L, Radtke Rodney A, Urban Thomas J, Cavalleri Gianpiero L, Depondt Chantal, Need Anna C, Walley Nicole M, Nicoletti Paola, Ge Dongliang, Catarino Claudia B, Duncan John S, Kasperaviciūte Dalia, Tate Sarah K, Caboclo Luis O, Sander Josemir W, Clayton Lisa, Linney Kristen N, Shianna Kevin V, Gumbs Curtis E, Smith Jason, Cronin Kenneth D, Maia Jessica M, Doherty Colin P, Pandolfo Massimo, Leppert David, Middleton Lefkos T, Gibson Rachel A, Johnson Michael R, Matthews Paul M, Hosford David, Kälviäinen Reetta, Eriksson Kai, Kantanen Anne-Mari, Dorn Thomas, Hansen Jörg, Krämer Günter, Steinhoff Bernhard J, Wieser Heinz-Gregor, Zumsteg Dominik, Ortega Marcos, Wood Nicholas W, Huxley-Jones Julie, Mikati Mohamad, Gallentine William B, Husain Aatif M, Buckley Patrick G, Stallings Ray L, Podgoreanu Mihai V, Delanty Norman, Sisodiya Sanjay M and Goldstein David B. Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes. : American journal of human genetics. 20100621.