APA aipamena

Meins, M., Lehmann, J., Gerresheim, F., Herchenbach, J., Hagedorn, M., Hameister, K., & Epplen, J. (2005). Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome. BMJ Group.

Chicago Style aipamena

Meins, M., J. Lehmann, F. Gerresheim, J. Herchenbach, M. Hagedorn, K. Hameister, and J. Epplen. Submicroscopic Duplication in Xq28 Causes Increased Expression of the MECP2 Gene in a Boy With Severe Mental Retardation and Features of Rett Syndrome. BMJ Group, 2005.

MLA aipamena

Meins, M., et al. Submicroscopic Duplication in Xq28 Causes Increased Expression of the MECP2 Gene in a Boy With Severe Mental Retardation and Features of Rett Syndrome. BMJ Group, 2005.