A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndrome.

MLA

Caputo, Viviana, et al. “A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre Syndrome.” American Journal of Human Genetics, vol. 90, no. 1, Jan. 2012, pp. 161–69. EBSCOhost, https://doi.org/10.1016/j.ajhg.2011.12.011.

APA

Caputo, V., Cianetti, L., Niceta, M., Carta, C., Ciolfi, A., Bocchinfuso, G., Carrani, E., Dentici, M. L., Biamino, E., Belligni, E., Garavelli, L., Boccone, L., Melis, D., Andria, G., Gelb, B. D., Stella, L., Silengo, M., Dallapiccola, B., & Tartaglia, M. (2012). A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndrome. American Journal of Human Genetics, 90(1), 161–169. https://doi.org/10.1016/j.ajhg.2011.12.011

Chicago

Caputo, Viviana, Luciano Cianetti, Marcello Niceta, Claudio Carta, Andrea Ciolfi, Gianfranco Bocchinfuso, Eugenio Carrani, et al. 2012. “A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre Syndrome.” American Journal of Human Genetics 90 (1): 161–69. doi:10.1016/j.ajhg.2011.12.011.