APA
Mirzaa G., Parry D. A., Fry A. E., Giamanco K. A., Schwartzentruber J., Vanstone M., Logan C. V., Roberts N., Johnson C. A., Singh S., Kholmanskikh S. S., Adams C., Hodge R. D., Hevner R. F., Bonthron D. T., Braun K. P. J., Faivre L., Rivière J., St-Onge J., Gripp K. W., Mancini G. M., Pang K., Sweeney E., van Esch H., Verbeek N., Wieczorek D., Steinraths M., Majewski J., Boycot K. M., Pilz D. T., Ross M. E., Dobyns W. B. & Sheridan E. G. (20140616). De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. : Nature genetics.
Chicago
Mirzaa Ghayda, Parry David A, Fry Andrew E, Giamanco Kristin A, Schwartzentruber Jeremy, Vanstone Megan, Logan Clare V, Roberts Nicola, Johnson Colin A, Singh Shawn, Kholmanskikh Stanislav S, Adams Carissa, Hodge Rebecca D, Hevner Robert F, Bonthron David T, Braun Kees P J, Faivre Laurence, Rivière Jean-Baptiste, St-Onge Judith, Gripp Karen W, Mancini Grazia Ms, Pang Ki, Sweeney Elizabeth, van Esch Hilde, Verbeek Nienke, Wieczorek Dagmar, Steinraths Michelle, Majewski Jacek, Boycot Kym M, Pilz Daniela T, Ross M Elizabeth, Dobyns William B and Sheridan Eamonn G. 20140616. De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. : Nature genetics.
Harvard
Mirzaa G., Parry D. A., Fry A. E., Giamanco K. A., Schwartzentruber J., Vanstone M., Logan C. V., Roberts N., Johnson C. A., Singh S., Kholmanskikh S. S., Adams C., Hodge R. D., Hevner R. F., Bonthron D. T., Braun K. P. J., Faivre L., Rivière J., St-Onge J., Gripp K. W., Mancini G. M., Pang K., Sweeney E., van Esch H., Verbeek N., Wieczorek D., Steinraths M., Majewski J., Boycot K. M., Pilz D. T., Ross M. E., Dobyns W. B. and Sheridan E. G. (20140616). De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. : Nature genetics.
MLA
Mirzaa Ghayda, Parry David A, Fry Andrew E, Giamanco Kristin A, Schwartzentruber Jeremy, Vanstone Megan, Logan Clare V, Roberts Nicola, Johnson Colin A, Singh Shawn, Kholmanskikh Stanislav S, Adams Carissa, Hodge Rebecca D, Hevner Robert F, Bonthron David T, Braun Kees P J, Faivre Laurence, Rivière Jean-Baptiste, St-Onge Judith, Gripp Karen W, Mancini Grazia Ms, Pang Ki, Sweeney Elizabeth, van Esch Hilde, Verbeek Nienke, Wieczorek Dagmar, Steinraths Michelle, Majewski Jacek, Boycot Kym M, Pilz Daniela T, Ross M Elizabeth, Dobyns William B and Sheridan Eamonn G. De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. : Nature genetics. 20140616.