APA
Jansen S., van der Werf I. M., Innes A. M., Afenjar A., Agrawal P. B., Anderson I. J., Atwal P. S., van Binsbergen E., van den Boogaard M., Castiglia L., Coban-Akdemir Z. H., van Dijck A., Doummar D., van Eerde A. M., van Essen A. J., van Gassen K. L., Guillen Sacoto M. J., van Haelst M. M., Iossifov I., Jackson J. L., Judd E., Kaiwar C., Keren B., Klee E. W., Klein Wassink-Ruiter J. S., Meuwissen M. E., Monaghan K. G., de Munnik S. A., Nava C., Ockeloen C. W., Pettinato R., Racher H., Rinne T., Romano C., Sanders V. R., Schnur R. E., Smeets E. J., Stegmann A. P. A., Stray-Pedersen A., Sweetser D. A., Terhal P. A., Tveten K., VanNoy G. E., de Vries P. F., Waxler J. L., Willing M., Pfundt R., Veltman J. A., Kooy R. F., Vissers L. E. L. M. & de Vries B. B. A. (20200612). De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms. : European journal of human genetics : EJHG.
Chicago
Jansen Sandra, van der Werf Ilse M, Innes A Micheil, Afenjar Alexandra, Agrawal Pankaj B, Anderson Ilse J, Atwal Paldeep S, van Binsbergen Ellen, van den Boogaard Marie-José, Castiglia Lucia, Coban-Akdemir Zeynep H, van Dijck Anke, Doummar Diane, van Eerde Albertien M, van Essen Anthonie J, van Gassen Koen L, Guillen Sacoto Maria J, van Haelst Mieke M, Iossifov Ivan, Jackson Jessica L, Judd Elizabeth, Kaiwar Charu, Keren Boris, Klee Eric W, Klein Wassink-Ruiter Jolien S, Meuwissen Marije E, Monaghan Kristin G, de Munnik Sonja A, Nava Caroline, Ockeloen Charlotte W, Pettinato Rosa, Racher Hilary, Rinne Tuula, Romano Corrado, Sanders Victoria R, Schnur Rhonda E, Smeets Eric J, Stegmann Alexander P A, Stray-Pedersen Asbjørg, Sweetser David A, Terhal Paulien A, Tveten Kristian, VanNoy Grace E, de Vries Petra F, Waxler Jessica L, Willing Marcia, Pfundt Rolph, Veltman Joris A, Kooy R Frank, Vissers Lisenka E L M and de Vries Bert B A. 20200612. De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms. : European journal of human genetics : EJHG.
Harvard
Jansen S., van der Werf I. M., Innes A. M., Afenjar A., Agrawal P. B., Anderson I. J., Atwal P. S., van Binsbergen E., van den Boogaard M., Castiglia L., Coban-Akdemir Z. H., van Dijck A., Doummar D., van Eerde A. M., van Essen A. J., van Gassen K. L., Guillen Sacoto M. J., van Haelst M. M., Iossifov I., Jackson J. L., Judd E., Kaiwar C., Keren B., Klee E. W., Klein Wassink-Ruiter J. S., Meuwissen M. E., Monaghan K. G., de Munnik S. A., Nava C., Ockeloen C. W., Pettinato R., Racher H., Rinne T., Romano C., Sanders V. R., Schnur R. E., Smeets E. J., Stegmann A. P. A., Stray-Pedersen A., Sweetser D. A., Terhal P. A., Tveten K., VanNoy G. E., de Vries P. F., Waxler J. L., Willing M., Pfundt R., Veltman J. A., Kooy R. F., Vissers L. E. L. M. and de Vries B. B. A. (20200612). De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms. : European journal of human genetics : EJHG.
MLA
Jansen Sandra, van der Werf Ilse M, Innes A Micheil, Afenjar Alexandra, Agrawal Pankaj B, Anderson Ilse J, Atwal Paldeep S, van Binsbergen Ellen, van den Boogaard Marie-José, Castiglia Lucia, Coban-Akdemir Zeynep H, van Dijck Anke, Doummar Diane, van Eerde Albertien M, van Essen Anthonie J, van Gassen Koen L, Guillen Sacoto Maria J, van Haelst Mieke M, Iossifov Ivan, Jackson Jessica L, Judd Elizabeth, Kaiwar Charu, Keren Boris, Klee Eric W, Klein Wassink-Ruiter Jolien S, Meuwissen Marije E, Monaghan Kristin G, de Munnik Sonja A, Nava Caroline, Ockeloen Charlotte W, Pettinato Rosa, Racher Hilary, Rinne Tuula, Romano Corrado, Sanders Victoria R, Schnur Rhonda E, Smeets Eric J, Stegmann Alexander P A, Stray-Pedersen Asbjørg, Sweetser David A, Terhal Paulien A, Tveten Kristian, VanNoy Grace E, de Vries Petra F, Waxler Jessica L, Willing Marcia, Pfundt Rolph, Veltman Joris A, Kooy R Frank, Vissers Lisenka E L M and de Vries Bert B A. De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms. : European journal of human genetics : EJHG. 20200612.