APA
Fry A. E., Fawcett K. A., Zelnik N., Yuan H., Thompson B. A. N., Shemer-Meiri L., Cushion T. D., Mugalaasi H., Sims D., Stoodley N., Chung S., Rees M. I., Patel C. V., Brueton L. A., Layet V., Giuliano F., Kerr M. P., Banne E., Meiner V., Lerman-Sagie T., Helbig K. L., Kofman L. H., Knight K. M., Chen W., Kannan V., Hu C., Kusumoto H., Zhang J., Swanger S. A., Shaulsky G. H., Mirzaa G. M., Muir A. M., Mefford H. C., Dobyns W. B., Mackenzie A. B., Mullins J. G. L., Lemke J. R., Bahi-Buisson N., Traynelis S. F., Iago H. F. & Pilz D. T. (20190627). De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. : Brain : a journal of neurology.
Chicago
Fry Andrew E, Fawcett Katherine A, Zelnik Nathanel, Yuan Hongjie, Thompson Belinda A N, Shemer-Meiri Lilach, Cushion Thomas D, Mugalaasi Hood, Sims David, Stoodley Neil, Chung Seo-Kyung, Rees Mark I, Patel Chirag V, Brueton Louise A, Layet Valérie, Giuliano Fabienne, Kerr Michael P, Banne Ehud, Meiner Vardiella, Lerman-Sagie Tally, Helbig Katherine L, Kofman Laura H, Knight Kristin M, Chen Wenjuan, Kannan Varun, Hu Chun, Kusumoto Hirofumi, Zhang Jin, Swanger Sharon A, Shaulsky Gil H, Mirzaa Ghayda M, Muir Alison M, Mefford Heather C, Dobyns William B, Mackenzie Amanda B, Mullins Jonathan G L, Lemke Johannes R, Bahi-Buisson Nadia, Traynelis Stephen F, Iago Heledd F and Pilz Daniela T. 20190627. De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. : Brain : a journal of neurology.
Harvard
Fry A. E., Fawcett K. A., Zelnik N., Yuan H., Thompson B. A. N., Shemer-Meiri L., Cushion T. D., Mugalaasi H., Sims D., Stoodley N., Chung S., Rees M. I., Patel C. V., Brueton L. A., Layet V., Giuliano F., Kerr M. P., Banne E., Meiner V., Lerman-Sagie T., Helbig K. L., Kofman L. H., Knight K. M., Chen W., Kannan V., Hu C., Kusumoto H., Zhang J., Swanger S. A., Shaulsky G. H., Mirzaa G. M., Muir A. M., Mefford H. C., Dobyns W. B., Mackenzie A. B., Mullins J. G. L., Lemke J. R., Bahi-Buisson N., Traynelis S. F., Iago H. F. and Pilz D. T. (20190627). De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. : Brain : a journal of neurology.
MLA
Fry Andrew E, Fawcett Katherine A, Zelnik Nathanel, Yuan Hongjie, Thompson Belinda A N, Shemer-Meiri Lilach, Cushion Thomas D, Mugalaasi Hood, Sims David, Stoodley Neil, Chung Seo-Kyung, Rees Mark I, Patel Chirag V, Brueton Louise A, Layet Valérie, Giuliano Fabienne, Kerr Michael P, Banne Ehud, Meiner Vardiella, Lerman-Sagie Tally, Helbig Katherine L, Kofman Laura H, Knight Kristin M, Chen Wenjuan, Kannan Varun, Hu Chun, Kusumoto Hirofumi, Zhang Jin, Swanger Sharon A, Shaulsky Gil H, Mirzaa Ghayda M, Muir Alison M, Mefford Heather C, Dobyns William B, Mackenzie Amanda B, Mullins Jonathan G L, Lemke Johannes R, Bahi-Buisson Nadia, Traynelis Stephen F, Iago Heledd F and Pilz Daniela T. De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. : Brain : a journal of neurology. 20190627.