APA
Lionel A. C., Tammimies K., Vaags A. K., Rosenfeld J. A., Ahn J. W., Merico D., Noor A., Runke C. K., Pillalamarri V. K., Carter M. T., Gazzellone M. J., Thiruvahindrapuram B., Fagerberg C., Laulund L. W., Pellecchia G., Lamoureux S., Deshpande C., Clayton-Smith J., White A. C., Leather S., Trounce J., Melanie Bedford H., Hatchwell E., Eis P. S., Yuen R. K. C., Walker S., Uddin M., Geraghty M. T., Nikkel S. M., Tomiak E. M., Fernandez B. A., Soreni N., Crosbie J., Arnold P. D., Schachar R. J., Roberts W., Paterson A. D., So J., Szatmari P., Chrysler C., Woodbury-Smith M., Brian Lowry R., Zwaigenbaum L., Mandyam D., Wei J., Macdonald J. R., Howe J. L., Nalpathamkalam T., Wang Z., Tolson D., Cobb D. S., Wilks T. M., Sorensen M. J., Bader P. I., An Y., Wu B., Musumeci S. A., Romano C., Postorivo D., Nardone A. M., Monica M. D., Scarano G., Zoccante L., Novara F., Zuffardi O., Ciccone R., Antona V., Carella M., Zelante L., Cavalli P., Poggiani C., Cavallari U., Argiropoulos B., Chernos J., Brasch-Andersen C., Speevak M., Fichera M., Ogilvie C. M., Shen Y., Hodge J. C., Talkowski M. E., Stavropoulos D. J., Marshall C. R. & Scherer S. W. (20141203). Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. : Human molecular genetics.
Chicago
Lionel Anath C, Tammimies Kristiina, Vaags Andrea K, Rosenfeld Jill A, Ahn Joo Wook, Merico Daniele, Noor Abdul, Runke Cassandra K, Pillalamarri Vamsee K, Carter Melissa T, Gazzellone Matthew J, Thiruvahindrapuram Bhooma, Fagerberg Christina, Laulund Lone W, Pellecchia Giovanna, Lamoureux Sylvia, Deshpande Charu, Clayton-Smith Jill, White Ann C, Leather Susan, Trounce John, Melanie Bedford H, Hatchwell Eli, Eis Peggy S, Yuen Ryan K C, Walker Susan, Uddin Mohammed, Geraghty Michael T, Nikkel Sarah M, Tomiak Eva M, Fernandez Bridget A, Soreni Noam, Crosbie Jennifer, Arnold Paul D, Schachar Russell J, Roberts Wendy, Paterson Andrew D, So Joyce, Szatmari Peter, Chrysler Christina, Woodbury-Smith Marc, Brian Lowry R, Zwaigenbaum Lonnie, Mandyam Divya, Wei John, Macdonald Jeffrey R, Howe Jennifer L, Nalpathamkalam Thomas, Wang Zhuozhi, Tolson Daniel, Cobb David S, Wilks Timothy M, Sorensen Mark J, Bader Patricia I, An Yu, Wu Bai-Lin, Musumeci Sebastiano Antonino, Romano Corrado, Postorivo Diana, Nardone Anna M, Monica Matteo Della, Scarano Gioacchino, Zoccante Leonardo, Novara Francesca, Zuffardi Orsetta, Ciccone Roberto, Antona Vincenzo, Carella Massimo, Zelante Leopoldo, Cavalli Pietro, Poggiani Carlo, Cavallari Ugo, Argiropoulos Bob, Chernos Judy, Brasch-Andersen Charlotte, Speevak Marsha, Fichera Marco, Ogilvie Caroline Mackie, Shen Yiping, Hodge Jennelle C, Talkowski Michael E, Stavropoulos Dimitri J, Marshall Christian R and Scherer Stephen W. 20141203. Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. : Human molecular genetics.
Harvard
Lionel A. C., Tammimies K., Vaags A. K., Rosenfeld J. A., Ahn J. W., Merico D., Noor A., Runke C. K., Pillalamarri V. K., Carter M. T., Gazzellone M. J., Thiruvahindrapuram B., Fagerberg C., Laulund L. W., Pellecchia G., Lamoureux S., Deshpande C., Clayton-Smith J., White A. C., Leather S., Trounce J., Melanie Bedford H., Hatchwell E., Eis P. S., Yuen R. K. C., Walker S., Uddin M., Geraghty M. T., Nikkel S. M., Tomiak E. M., Fernandez B. A., Soreni N., Crosbie J., Arnold P. D., Schachar R. J., Roberts W., Paterson A. D., So J., Szatmari P., Chrysler C., Woodbury-Smith M., Brian Lowry R., Zwaigenbaum L., Mandyam D., Wei J., Macdonald J. R., Howe J. L., Nalpathamkalam T., Wang Z., Tolson D., Cobb D. S., Wilks T. M., Sorensen M. J., Bader P. I., An Y., Wu B., Musumeci S. A., Romano C., Postorivo D., Nardone A. M., Monica M. D., Scarano G., Zoccante L., Novara F., Zuffardi O., Ciccone R., Antona V., Carella M., Zelante L., Cavalli P., Poggiani C., Cavallari U., Argiropoulos B., Chernos J., Brasch-Andersen C., Speevak M., Fichera M., Ogilvie C. M., Shen Y., Hodge J. C., Talkowski M. E., Stavropoulos D. J., Marshall C. R. and Scherer S. W. (20141203). Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. : Human molecular genetics.
MLA
Lionel Anath C, Tammimies Kristiina, Vaags Andrea K, Rosenfeld Jill A, Ahn Joo Wook, Merico Daniele, Noor Abdul, Runke Cassandra K, Pillalamarri Vamsee K, Carter Melissa T, Gazzellone Matthew J, Thiruvahindrapuram Bhooma, Fagerberg Christina, Laulund Lone W, Pellecchia Giovanna, Lamoureux Sylvia, Deshpande Charu, Clayton-Smith Jill, White Ann C, Leather Susan, Trounce John, Melanie Bedford H, Hatchwell Eli, Eis Peggy S, Yuen Ryan K C, Walker Susan, Uddin Mohammed, Geraghty Michael T, Nikkel Sarah M, Tomiak Eva M, Fernandez Bridget A, Soreni Noam, Crosbie Jennifer, Arnold Paul D, Schachar Russell J, Roberts Wendy, Paterson Andrew D, So Joyce, Szatmari Peter, Chrysler Christina, Woodbury-Smith Marc, Brian Lowry R, Zwaigenbaum Lonnie, Mandyam Divya, Wei John, Macdonald Jeffrey R, Howe Jennifer L, Nalpathamkalam Thomas, Wang Zhuozhi, Tolson Daniel, Cobb David S, Wilks Timothy M, Sorensen Mark J, Bader Patricia I, An Yu, Wu Bai-Lin, Musumeci Sebastiano Antonino, Romano Corrado, Postorivo Diana, Nardone Anna M, Monica Matteo Della, Scarano Gioacchino, Zoccante Leonardo, Novara Francesca, Zuffardi Orsetta, Ciccone Roberto, Antona Vincenzo, Carella Massimo, Zelante Leopoldo, Cavalli Pietro, Poggiani Carlo, Cavallari Ugo, Argiropoulos Bob, Chernos Judy, Brasch-Andersen Charlotte, Speevak Marsha, Fichera Marco, Ogilvie Caroline Mackie, Shen Yiping, Hodge Jennelle C, Talkowski Michael E, Stavropoulos Dimitri J, Marshall Christian R and Scherer Stephen W. Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. : Human molecular genetics. 20141203.