Style de citation APA (7e éd.)

Bochukova, E., Roscioli, T., Hedges, D., Taylor, I., Johnson, D., David, D., . . . Wilkie, A. (2009). Rare mutations of FGFR2 causing apert syndrome: Identification of the first partial gene deletion, and an Alu element insertion from a new subfamily.

Style de citation Chicago (17e éd.)

Bochukova, E., T. Roscioli, D. Hedges, I. Taylor, D. Johnson, D. David, P. Deininger, et A. Wilkie. Rare Mutations of FGFR2 Causing Apert Syndrome: Identification of the First Partial Gene Deletion, and an Alu Element Insertion from a New Subfamily. 2009.

Style de citation MLA (9e éd.)

Bochukova, E., et al. Rare Mutations of FGFR2 Causing Apert Syndrome: Identification of the First Partial Gene Deletion, and an Alu Element Insertion from a New Subfamily. 2009.