APA

van Bon B. W. M., Mefford H. C., Menten B., Koolen D. A., Sharp A. J., Nillesen W. M., Innis J. W., de Ravel T. J. L., Mercer C. L., Fichera M., Stewart H., Connell L. E., Ounap K., Lachlan K., Castle B., Van der Aa N., van Ravenswaaij C., Nobrega M. A., Serra-Juhé C., Simonic I., de Leeuw N., Pfundt R., Bongers E. M., Baker C., Finnemore P., Huang S., Maloney V. K., Crolla J. A., van Kalmthout M., Elia M., Vandeweyer G., Fryns J. P., Janssens S., Foulds N., Reitano S., Smith K., Parkel S., Loeys B., Woods C. G., Oostra A., Speleman F., Pereira A. C., Kurg A., Willatt L., Knight S. J. L., Vermeesch J. R., Romano C., Barber J. C., Mortier G., Pérez-Jurado L. A., Kooy F., Brunner H. G., Eichler E. E., Kleefstra T. & de Vries B. B. A. (20091102). Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. : Journal of medical genetics.

Chicago

van Bon B W M, Mefford H C, Menten B, Koolen D A, Sharp A J, Nillesen W M, Innis J W, de Ravel T J L, Mercer C L, Fichera M, Stewart H, Connell L E, Ounap K, Lachlan K, Castle B, Van der Aa N, van Ravenswaaij C, Nobrega M A, Serra-Juhé C, Simonic I, de Leeuw N, Pfundt R, Bongers E M, Baker C, Finnemore P, Huang S, Maloney V K, Crolla J A, van Kalmthout M, Elia M, Vandeweyer G, Fryns J P, Janssens S, Foulds N, Reitano S, Smith K, Parkel S, Loeys B, Woods C G, Oostra A, Speleman F, Pereira A C, Kurg A, Willatt L, Knight S J L, Vermeesch J R, Romano C, Barber J C, Mortier G, Pérez-Jurado L A, Kooy F, Brunner H G, Eichler E E, Kleefstra T and de Vries B B A. 20091102. Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. : Journal of medical genetics.

Harvard

van Bon B. W. M., Mefford H. C., Menten B., Koolen D. A., Sharp A. J., Nillesen W. M., Innis J. W., de Ravel T. J. L., Mercer C. L., Fichera M., Stewart H., Connell L. E., Ounap K., Lachlan K., Castle B., Van der Aa N., van Ravenswaaij C., Nobrega M. A., Serra-Juhé C., Simonic I., de Leeuw N., Pfundt R., Bongers E. M., Baker C., Finnemore P., Huang S., Maloney V. K., Crolla J. A., van Kalmthout M., Elia M., Vandeweyer G., Fryns J. P., Janssens S., Foulds N., Reitano S., Smith K., Parkel S., Loeys B., Woods C. G., Oostra A., Speleman F., Pereira A. C., Kurg A., Willatt L., Knight S. J. L., Vermeesch J. R., Romano C., Barber J. C., Mortier G., Pérez-Jurado L. A., Kooy F., Brunner H. G., Eichler E. E., Kleefstra T. and de Vries B. B. A. (20091102). Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. : Journal of medical genetics.

MLA

van Bon B W M, Mefford H C, Menten B, Koolen D A, Sharp A J, Nillesen W M, Innis J W, de Ravel T J L, Mercer C L, Fichera M, Stewart H, Connell L E, Ounap K, Lachlan K, Castle B, Van der Aa N, van Ravenswaaij C, Nobrega M A, Serra-Juhé C, Simonic I, de Leeuw N, Pfundt R, Bongers E M, Baker C, Finnemore P, Huang S, Maloney V K, Crolla J A, van Kalmthout M, Elia M, Vandeweyer G, Fryns J P, Janssens S, Foulds N, Reitano S, Smith K, Parkel S, Loeys B, Woods C G, Oostra A, Speleman F, Pereira A C, Kurg A, Willatt L, Knight S J L, Vermeesch J R, Romano C, Barber J C, Mortier G, Pérez-Jurado L A, Kooy F, Brunner H G, Eichler E E, Kleefstra T and de Vries B B A. Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. : Journal of medical genetics. 20091102.