APA

van Bon B. W. M., Koolen D. A., Borgatti R., Magee A., Garcia-Minaur S., Rooms L., Reardon W., Zollino M., Bonaglia M. C., De Gregori M., Novara F., Grasso R., Ciccone R., van Duyvenvoorde H. A., Aalbers A. M., Guerrini R., Fazzi E., Nillesen W. M., McCullough S., Kant S. G., Marcelis C. L., Pfundt R., de Leeuw N., Smeets D., Sistermans E. A., Wit J. M., Hamel B. C., Brunner H. G., Kooy F., Zuffardi O. & de Vries B. B. A. (20080811). Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis. : Journal of medical genetics.

Chicago

van Bon B W M, Koolen D A, Borgatti R, Magee A, Garcia-Minaur S, Rooms L, Reardon W, Zollino M, Bonaglia M C, De Gregori M, Novara F, Grasso R, Ciccone R, van Duyvenvoorde H A, Aalbers A M, Guerrini R, Fazzi E, Nillesen W M, McCullough S, Kant S G, Marcelis C L, Pfundt R, de Leeuw N, Smeets D, Sistermans E A, Wit J M, Hamel B C, Brunner H G, Kooy F, Zuffardi O and de Vries B B A. 20080811. Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis. : Journal of medical genetics.

Harvard

van Bon B. W. M., Koolen D. A., Borgatti R., Magee A., Garcia-Minaur S., Rooms L., Reardon W., Zollino M., Bonaglia M. C., De Gregori M., Novara F., Grasso R., Ciccone R., van Duyvenvoorde H. A., Aalbers A. M., Guerrini R., Fazzi E., Nillesen W. M., McCullough S., Kant S. G., Marcelis C. L., Pfundt R., de Leeuw N., Smeets D., Sistermans E. A., Wit J. M., Hamel B. C., Brunner H. G., Kooy F., Zuffardi O. and de Vries B. B. A. (20080811). Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis. : Journal of medical genetics.

MLA

van Bon B W M, Koolen D A, Borgatti R, Magee A, Garcia-Minaur S, Rooms L, Reardon W, Zollino M, Bonaglia M C, De Gregori M, Novara F, Grasso R, Ciccone R, van Duyvenvoorde H A, Aalbers A M, Guerrini R, Fazzi E, Nillesen W M, McCullough S, Kant S G, Marcelis C L, Pfundt R, de Leeuw N, Smeets D, Sistermans E A, Wit J M, Hamel B C, Brunner H G, Kooy F, Zuffardi O and de Vries B B A. Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis. : Journal of medical genetics. 20080811.