APA

de Greef J. C., Krom Y. D., den Hamer B., Snider L., Hiramuki Y., van den Akker R. F. P., Breslin K., Pakusch M., Salvatori D. C. F., Slütter B., Tawil R., Blewitt M. E., Tapscott S. J. & van der Maarel S. M. (20190107). Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model. : Human molecular genetics.

Chicago

de Greef Jessica C, Krom Yvonne D, den Hamer Bianca, Snider Lauren, Hiramuki Yosuke, van den Akker Rob F P, Breslin Kelsey, Pakusch Miha, Salvatori Daniela C F, Slütter Bram, Tawil Rabi, Blewitt Marnie E, Tapscott Stephen J and van der Maarel Silvère M. 20190107. Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model. : Human molecular genetics.

Harvard

de Greef J. C., Krom Y. D., den Hamer B., Snider L., Hiramuki Y., van den Akker R. F. P., Breslin K., Pakusch M., Salvatori D. C. F., Slütter B., Tawil R., Blewitt M. E., Tapscott S. J. and van der Maarel S. M. (20190107). Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model. : Human molecular genetics.

MLA

de Greef Jessica C, Krom Yvonne D, den Hamer Bianca, Snider Lauren, Hiramuki Yosuke, van den Akker Rob F P, Breslin Kelsey, Pakusch Miha, Salvatori Daniela C F, Slütter Bram, Tawil Rabi, Blewitt Marnie E, Tapscott Stephen J and van der Maarel Silvère M. Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model. : Human molecular genetics. 20190107.