APA

Risheg H., Graham J. M., Clark R. D., Rogers R. C., Opitz J. M., Moeschler J. B., Peiffer A. P., May M., Joseph S. M., Jones J. R., Stevenson R. E., Schwartz C. E. & Friez M. J. (20070606). A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome. : Nature genetics.

Chicago

Risheg Hiba, Graham John M, Clark Robin D, Rogers R Curtis, Opitz John M, Moeschler John B, Peiffer Andreas P, May Melanie, Joseph Sumy M, Jones Julie R, Stevenson Roger E, Schwartz Charles E and Friez Michael J. 20070606. A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome. : Nature genetics.

Harvard

Risheg H., Graham J. M., Clark R. D., Rogers R. C., Opitz J. M., Moeschler J. B., Peiffer A. P., May M., Joseph S. M., Jones J. R., Stevenson R. E., Schwartz C. E. and Friez M. J. (20070606). A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome. : Nature genetics.

MLA

Risheg Hiba, Graham John M, Clark Robin D, Rogers R Curtis, Opitz John M, Moeschler John B, Peiffer Andreas P, May Melanie, Joseph Sumy M, Jones Julie R, Stevenson Roger E, Schwartz Charles E and Friez Michael J. A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome. : Nature genetics. 20070606.