APA引文

Roche, E. F., McGowan, A., Koulouri, O., Turgeon, M., Nicholas, A. K., Heffernan, E., . . . Schoenmakers, N. (2018). A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome. Clin Endocrinol (Oxf).

Citação norma Chicago

Roche, Edna F., et al. "A Novel IGSF1 Mutation in a Large Irish Kindred Highlights the Need for Familial Screening in the IGSF1 Deficiency Syndrome." Clin Endocrinol (Oxf) 2018.

MLA引文

Roche, Edna F., et al. "A Novel IGSF1 Mutation in a Large Irish Kindred Highlights the Need for Familial Screening in the IGSF1 Deficiency Syndrome." Clin Endocrinol (Oxf) 2018.