APA

van Bon B. W. M., Koolen D. A., Brueton L., McMullan D., Lichtenbelt K. D., Adès L. C., Peters G., Gibson K., Moloney S., Novara F., Pramparo T., Dalla Bernardina B., Zoccante L., Balottin U., Piazza F., Pecile V., Gasparini P., Guerci V., Kets M., Pfundt R., de Brouwer A. P., Veltman J. A., de Leeuw N., Wilson M., Antony J., Reitano S., Luciano D., Fichera M., Romano C., Brunner H. G., Zuffardi O. & de Vries B. B. A. (20100224). The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype. : European journal of human genetics : EJHG.

Chicago

van Bon Bregje W M, Koolen David A, Brueton Louise, McMullan Dominic, Lichtenbelt Klaske D, Adès Lesley C, Peters Gregory, Gibson Kate, Moloney Susan, Novara Francesca, Pramparo Tiziano, Dalla Bernardina Bernardo, Zoccante Leonardo, Balottin Umberto, Piazza Fausta, Pecile Vanna, Gasparini Paolo, Guerci Veronica, Kets Marleen, Pfundt Rolph, de Brouwer Arjan P, Veltman Joris A, de Leeuw Nicole, Wilson Meredith, Antony Jayne, Reitano Santina, Luciano Daniela, Fichera Marco, Romano Corrado, Brunner Han G, Zuffardi Orsetta and de Vries Bert B A. 20100224. The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype. : European journal of human genetics : EJHG.

Harvard

van Bon B. W. M., Koolen D. A., Brueton L., McMullan D., Lichtenbelt K. D., Adès L. C., Peters G., Gibson K., Moloney S., Novara F., Pramparo T., Dalla Bernardina B., Zoccante L., Balottin U., Piazza F., Pecile V., Gasparini P., Guerci V., Kets M., Pfundt R., de Brouwer A. P., Veltman J. A., de Leeuw N., Wilson M., Antony J., Reitano S., Luciano D., Fichera M., Romano C., Brunner H. G., Zuffardi O. and de Vries B. B. A. (20100224). The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype. : European journal of human genetics : EJHG.

MLA

van Bon Bregje W M, Koolen David A, Brueton Louise, McMullan Dominic, Lichtenbelt Klaske D, Adès Lesley C, Peters Gregory, Gibson Kate, Moloney Susan, Novara Francesca, Pramparo Tiziano, Dalla Bernardina Bernardo, Zoccante Leonardo, Balottin Umberto, Piazza Fausta, Pecile Vanna, Gasparini Paolo, Guerci Veronica, Kets Marleen, Pfundt Rolph, de Brouwer Arjan P, Veltman Joris A, de Leeuw Nicole, Wilson Meredith, Antony Jayne, Reitano Santina, Luciano Daniela, Fichera Marco, Romano Corrado, Brunner Han G, Zuffardi Orsetta and de Vries Bert B A. The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype. : European journal of human genetics : EJHG. 20100224.