APA (7th ed.) Citation

Steiner, M., Steiner, B., Rolfs, A., Wangnick, M., Burstein, C., Freund, M., & Schuff-Werner, P. (2005). Antithrombin gene mutation 5356-5364*delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin a-helix D molecular pathology. Annals of Hematology, 84(1), 56. https://doi.org/10.1007/s00277-004-0906-3

Chicago Style (17th ed.) Citation

Steiner, M., B. Steiner, A. Rolfs, M. Wangnick, C. Burstein, M. Freund, and P. Schuff-Werner. "Antithrombin Gene Mutation 5356-5364*delCTT with Type I Deficiency and Early-onset Thrombophilia and a Brief Review of the Antithrombin A-helix D Molecular Pathology." Annals of Hematology 84, no. 1 (2005): 56. https://doi.org/10.1007/s00277-004-0906-3.

MLA (9th ed.) Citation

Steiner, M., et al. "Antithrombin Gene Mutation 5356-5364*delCTT with Type I Deficiency and Early-onset Thrombophilia and a Brief Review of the Antithrombin A-helix D Molecular Pathology." Annals of Hematology, vol. 84, no. 1, 2005, p. 56, https://doi.org/10.1007/s00277-004-0906-3.