APA
Tartaglia M., Pennacchio L. A., Zhao C., Yadav K. K., Fodale V., Sarkozy A., Pandit B., Oishi K., Martinelli S., Schackwitz W., Ustaszewska A., Martin J., Bristow J., Carta C., Lepri F., Neri C., Vasta I., Gibson K., Curry C. J., Siguero J. P. L., Digilio M. C., Zampino G., Dallapiccola B., Bar-Sagi D. & Gelb B. D. (20070221). Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. : Nature genetics.
Chicago
Tartaglia Marco, Pennacchio Len A, Zhao Chen, Yadav Kamlesh K, Fodale Valentina, Sarkozy Anna, Pandit Bhaswati, Oishi Kimihiko, Martinelli Simone, Schackwitz Wendy, Ustaszewska Anna, Martin Joel, Bristow James, Carta Claudio, Lepri Francesca, Neri Cinzia, Vasta Isabella, Gibson Kate, Curry Cynthia J, Siguero Juan Pedro López, Digilio Maria Cristina, Zampino Giuseppe, Dallapiccola Bruno, Bar-Sagi Dafna and Gelb Bruce D. 20070221. Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. : Nature genetics.
Harvard
Tartaglia M., Pennacchio L. A., Zhao C., Yadav K. K., Fodale V., Sarkozy A., Pandit B., Oishi K., Martinelli S., Schackwitz W., Ustaszewska A., Martin J., Bristow J., Carta C., Lepri F., Neri C., Vasta I., Gibson K., Curry C. J., Siguero J. P. L., Digilio M. C., Zampino G., Dallapiccola B., Bar-Sagi D. and Gelb B. D. (20070221). Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. : Nature genetics.
MLA
Tartaglia Marco, Pennacchio Len A, Zhao Chen, Yadav Kamlesh K, Fodale Valentina, Sarkozy Anna, Pandit Bhaswati, Oishi Kimihiko, Martinelli Simone, Schackwitz Wendy, Ustaszewska Anna, Martin Joel, Bristow James, Carta Claudio, Lepri Francesca, Neri Cinzia, Vasta Isabella, Gibson Kate, Curry Cynthia J, Siguero Juan Pedro López, Digilio Maria Cristina, Zampino Giuseppe, Dallapiccola Bruno, Bar-Sagi Dafna and Gelb Bruce D. Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. : Nature genetics. 20070221.