APA
Capri Y., Flex E., Krumbach O. H. F., Carpentieri G., Cecchetti S., Lißewski C., Rezaei Adariani S., Schanze D., Brinkmann J., Piard J., Pantaleoni F., Lepri F. R., Goh E. S., Chong K., Stieglitz E., Meyer J., Kuechler A., Bramswig N. C., Sacharow S., Strullu M., Vial Y., Vignal C., Kensah G., Cuturilo G., Kazemein Jasemi N. S., Dvorsky R., Monaghan K. G., Vincent L. M., Cavé H., Verloes A., Ahmadian M. R., Tartaglia M. & Zenker M. (20200311). Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome. : American journal of human genetics.
Chicago
Capri Yline, Flex Elisabetta, Krumbach Oliver H F, Carpentieri Giovanna, Cecchetti Serena, Lißewski Christina, Rezaei Adariani Soheila, Schanze Denny, Brinkmann Julia, Piard Juliette, Pantaleoni Francesca, Lepri Francesca R, Goh Elaine Suk-Ying, Chong Karen, Stieglitz Elliot, Meyer Julia, Kuechler Alma, Bramswig Nuria C, Sacharow Stephanie, Strullu Marion, Vial Yoann, Vignal Cédric, Kensah George, Cuturilo Goran, Kazemein Jasemi Neda S, Dvorsky Radovan, Monaghan Kristin G, Vincent Lisa M, Cavé Hélène, Verloes Alain, Ahmadian Mohammad R, Tartaglia Marco and Zenker Martin. 20200311. Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome. : American journal of human genetics.
Harvard
Capri Y., Flex E., Krumbach O. H. F., Carpentieri G., Cecchetti S., Lißewski C., Rezaei Adariani S., Schanze D., Brinkmann J., Piard J., Pantaleoni F., Lepri F. R., Goh E. S., Chong K., Stieglitz E., Meyer J., Kuechler A., Bramswig N. C., Sacharow S., Strullu M., Vial Y., Vignal C., Kensah G., Cuturilo G., Kazemein Jasemi N. S., Dvorsky R., Monaghan K. G., Vincent L. M., Cavé H., Verloes A., Ahmadian M. R., Tartaglia M. and Zenker M. (20200311). Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome. : American journal of human genetics.
MLA
Capri Yline, Flex Elisabetta, Krumbach Oliver H F, Carpentieri Giovanna, Cecchetti Serena, Lißewski Christina, Rezaei Adariani Soheila, Schanze Denny, Brinkmann Julia, Piard Juliette, Pantaleoni Francesca, Lepri Francesca R, Goh Elaine Suk-Ying, Chong Karen, Stieglitz Elliot, Meyer Julia, Kuechler Alma, Bramswig Nuria C, Sacharow Stephanie, Strullu Marion, Vial Yoann, Vignal Cédric, Kensah George, Cuturilo Goran, Kazemein Jasemi Neda S, Dvorsky Radovan, Monaghan Kristin G, Vincent Lisa M, Cavé Hélène, Verloes Alain, Ahmadian Mohammad R, Tartaglia Marco and Zenker Martin. Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome. : American journal of human genetics. 20200311.