Cite
Severe Hb S-beta zero-thalassaemia with a T----C substitution in the donor splice site of the first intron of the beta-globin gene.
MLA
Gonzalez-Redondo, J. M., et al. “Severe Hb S-Beta Zero-Thalassaemia with a T----C Substitution in the Donor Splice Site of the First Intron of the Beta-Globin Gene.” British Journal of Haematology, vol. 71, no. 1, Jan. 1989, pp. 113–17. EBSCOhost, https://doi.org/10.1111/j.1365-2141.1989.tb06283.x.
APA
Gonzalez-Redondo, J. M., Stoming, T. A., Kutlar, F., Kutlar, A., McKie, V. C., McKie, K. M., & Huisman, T. H. (1989). Severe Hb S-beta zero-thalassaemia with a T----C substitution in the donor splice site of the first intron of the beta-globin gene. British Journal of Haematology, 71(1), 113–117. https://doi.org/10.1111/j.1365-2141.1989.tb06283.x
Chicago
Gonzalez-Redondo, J M, T A Stoming, F Kutlar, A Kutlar, V C McKie, K M McKie, and T H Huisman. 1989. “Severe Hb S-Beta Zero-Thalassaemia with a T----C Substitution in the Donor Splice Site of the First Intron of the Beta-Globin Gene.” British Journal of Haematology 71 (1): 113–17. doi:10.1111/j.1365-2141.1989.tb06283.x.