APA
Huckert M., Stoetzel C., Morkmued S., Laugel-Haushalter V., Geoffroy V., Muller J., Clauss F., Prasad M. K., Obry F., Raymond J. L., Switala M., Alembik Y., Soskin S., Mathieu E., Hemmerlé J., Weickert J., Dabovic B. B., Rifkin D. B., Dheedene A., Boudin E., Caluseriu O., Cholette M., Mcleod R., Antequera R., Gellé M., Coeuriot J., Jacquelin L., Bailleul-Forestier I., Manière M., Van Hul W., Bertola D., Dollé P., Verloes A., Mortier G., Dollfus H. & Bloch-Zupan A. (20160216). Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta. : Human molecular genetics.
Chicago
Huckert Mathilde, Stoetzel Corinne, Morkmued Supawich, Laugel-Haushalter Virginie, Geoffroy Véronique, Muller Jean, Clauss François, Prasad Megana K, Obry Frédéric, Raymond Jean Louis, Switala Marzena, Alembik Yves, Soskin Sylvie, Mathieu Eric, Hemmerlé Joseph, Weickert Jean-Luc, Dabovic Branka Brukner, Rifkin Daniel B, Dheedene Annelies, Boudin Eveline, Caluseriu Oana, Cholette Marie-Claude, Mcleod Ross, Antequera Reynaldo, Gellé Marie-Paule, Coeuriot Jean-Louis, Jacquelin Louis-Frédéric, Bailleul-Forestier Isabelle, Manière Marie-Cécile, Van Hul Wim, Bertola Debora, Dollé Pascal, Verloes Alain, Mortier Geert, Dollfus Hélène and Bloch-Zupan Agnès. 20160216. Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta. : Human molecular genetics.
Harvard
Huckert M., Stoetzel C., Morkmued S., Laugel-Haushalter V., Geoffroy V., Muller J., Clauss F., Prasad M. K., Obry F., Raymond J. L., Switala M., Alembik Y., Soskin S., Mathieu E., Hemmerlé J., Weickert J., Dabovic B. B., Rifkin D. B., Dheedene A., Boudin E., Caluseriu O., Cholette M., Mcleod R., Antequera R., Gellé M., Coeuriot J., Jacquelin L., Bailleul-Forestier I., Manière M., Van Hul W., Bertola D., Dollé P., Verloes A., Mortier G., Dollfus H. and Bloch-Zupan A. (20160216). Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta. : Human molecular genetics.
MLA
Huckert Mathilde, Stoetzel Corinne, Morkmued Supawich, Laugel-Haushalter Virginie, Geoffroy Véronique, Muller Jean, Clauss François, Prasad Megana K, Obry Frédéric, Raymond Jean Louis, Switala Marzena, Alembik Yves, Soskin Sylvie, Mathieu Eric, Hemmerlé Joseph, Weickert Jean-Luc, Dabovic Branka Brukner, Rifkin Daniel B, Dheedene Annelies, Boudin Eveline, Caluseriu Oana, Cholette Marie-Claude, Mcleod Ross, Antequera Reynaldo, Gellé Marie-Paule, Coeuriot Jean-Louis, Jacquelin Louis-Frédéric, Bailleul-Forestier Isabelle, Manière Marie-Cécile, Van Hul Wim, Bertola Debora, Dollé Pascal, Verloes Alain, Mortier Geert, Dollfus Hélène and Bloch-Zupan Agnès. Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta. : Human molecular genetics. 20160216.