APA
Palmer E. E., Stuhlmann T., Weinert S., Haan E., Van Esch H., Holvoet M., Boyle J., Leffler M., Raynaud M., Moraine C., van Bokhoven H., Kleefstra T., Kahrizi K., Najmabadi H., Ropers H., Delgado M. R., Sirsi D., Golla S., Sommer A., Pietryga M. P., Chung W. K., Wynn J., Rohena L., Bernardo E., Hamlin D., Faux B. M., Grange D. K., Manwaring L., Tolmie J., Joss S., Cobben J. M., Duijkers F. A. M., Goehringer J. M., Challman T. D., Hennig F., Fischer U., Grimme A., Suckow V., Musante L., Nicholl J., Shaw M., Lodh S. P., Niu Z., Rosenfeld J. A., Stankiewicz P., Jentsch T. J., Gecz J., Field M. & Kalscheuer V. M. (20190215). De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. : Molecular psychiatry.
Chicago
Palmer E E, Stuhlmann T, Weinert S, Haan E, Van Esch H, Holvoet M, Boyle J, Leffler M, Raynaud M, Moraine C, van Bokhoven H, Kleefstra T, Kahrizi K, Najmabadi H, Ropers H-H, Delgado M R, Sirsi D, Golla S, Sommer A, Pietryga M P, Chung W K, Wynn J, Rohena L, Bernardo E, Hamlin D, Faux B M, Grange D K, Manwaring L, Tolmie J, Joss S, Cobben J M, Duijkers F A M, Goehringer J M, Challman T D, Hennig F, Fischer U, Grimme A, Suckow V, Musante L, Nicholl J, Shaw M, Lodh S P, Niu Z, Rosenfeld J A, Stankiewicz P, Jentsch T J, Gecz J, Field M and Kalscheuer V M. 20190215. De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. : Molecular psychiatry.
Harvard
Palmer E. E., Stuhlmann T., Weinert S., Haan E., Van Esch H., Holvoet M., Boyle J., Leffler M., Raynaud M., Moraine C., van Bokhoven H., Kleefstra T., Kahrizi K., Najmabadi H., Ropers H., Delgado M. R., Sirsi D., Golla S., Sommer A., Pietryga M. P., Chung W. K., Wynn J., Rohena L., Bernardo E., Hamlin D., Faux B. M., Grange D. K., Manwaring L., Tolmie J., Joss S., Cobben J. M., Duijkers F. A. M., Goehringer J. M., Challman T. D., Hennig F., Fischer U., Grimme A., Suckow V., Musante L., Nicholl J., Shaw M., Lodh S. P., Niu Z., Rosenfeld J. A., Stankiewicz P., Jentsch T. J., Gecz J., Field M. and Kalscheuer V. M. (20190215). De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. : Molecular psychiatry.
MLA
Palmer E E, Stuhlmann T, Weinert S, Haan E, Van Esch H, Holvoet M, Boyle J, Leffler M, Raynaud M, Moraine C, van Bokhoven H, Kleefstra T, Kahrizi K, Najmabadi H, Ropers H-H, Delgado M R, Sirsi D, Golla S, Sommer A, Pietryga M P, Chung W K, Wynn J, Rohena L, Bernardo E, Hamlin D, Faux B M, Grange D K, Manwaring L, Tolmie J, Joss S, Cobben J M, Duijkers F A M, Goehringer J M, Challman T D, Hennig F, Fischer U, Grimme A, Suckow V, Musante L, Nicholl J, Shaw M, Lodh S P, Niu Z, Rosenfeld J A, Stankiewicz P, Jentsch T J, Gecz J, Field M and Kalscheuer V M. De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. : Molecular psychiatry. 20190215.