APA

Atik T., Koparir A., Bademci G., Foster J., Altunoglu U., Mutlu G. Y., Bowdin S., Elcioglu N., Tayfun G. A., Atik S. S., Ozen M., Ozkinay F., Alanay Y., Kayserili H., Thiel S. & Tekin M. (20160706). Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome. : Orphanet journal of rare diseases.

Chicago

Atik Tahir, Koparir Asuman, Bademci Guney, Foster Joseph, Altunoglu Umut, Mutlu Gül Yesiltepe, Bowdin Sarah, Elcioglu Nursel, Tayfun Gulsen A, Atik Sevinc Sahin, Ozen Mustafa, Ozkinay Ferda, Alanay Yasemin, Kayserili Hulya, Thiel Steffen and Tekin Mustafa. 20160706. Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome. : Orphanet journal of rare diseases.

Harvard

Atik T., Koparir A., Bademci G., Foster J., Altunoglu U., Mutlu G. Y., Bowdin S., Elcioglu N., Tayfun G. A., Atik S. S., Ozen M., Ozkinay F., Alanay Y., Kayserili H., Thiel S. and Tekin M. (20160706). Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome. : Orphanet journal of rare diseases.

MLA

Atik Tahir, Koparir Asuman, Bademci Guney, Foster Joseph, Altunoglu Umut, Mutlu Gül Yesiltepe, Bowdin Sarah, Elcioglu Nursel, Tayfun Gulsen A, Atik Sevinc Sahin, Ozen Mustafa, Ozkinay Ferda, Alanay Yasemin, Kayserili Hulya, Thiel Steffen and Tekin Mustafa. Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome. : Orphanet journal of rare diseases. 20160706.