APA ציטוט

Saal, H. M., Prows, C. A., Guerreiro, I., Donlin, M., Knudson, L., Sund, K. L., . . . Stottmann, R. W. (2015). A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia. Hum Mol Genet.

Citação norma Chicago

Saal, Howard M., Cynthia A. Prows, Iris Guerreiro, Milene Donlin, Luke Knudson, Kristen L. Sund, Ching-Fang Chang, Samantha A. Brugmann, and Rolf W. Stottmann. "A Mutation in FRIZZLED2 Impairs Wnt Signaling and Causes Autosomal Dominant Omodysplasia." Hum Mol Genet 2015.

ציטוט MLA

Saal, Howard M., et al. "A Mutation in FRIZZLED2 Impairs Wnt Signaling and Causes Autosomal Dominant Omodysplasia." Hum Mol Genet 2015.