Παραπομπή σε μορφή APA (7η εκδ.)

Shield, J., Flanagan, S., Mackay, D., Harries, L., Proks, P., Girard, C., . . . Ellard, S. (2008). Mosaic paternal uniparental isodisomy and an ABCC8 gene mutation in a patient with permanent neonatal diabetes and hemihypertrophy.

Παραπομπή σε μορφή Chicago (17η εκδ.)

Shield, J., SE Flanagan, D. Mackay, L. Harries, P. Proks, C. Girard, F. Ashcroft, I. Temple, και S. Ellard. Mosaic Paternal Uniparental Isodisomy and an ABCC8 Gene Mutation in a Patient with Permanent Neonatal Diabetes and Hemihypertrophy. 2008.

Παραπομπή σε μορφή MLA (9th εκδ.)

Shield, J., et al. Mosaic Paternal Uniparental Isodisomy and an ABCC8 Gene Mutation in a Patient with Permanent Neonatal Diabetes and Hemihypertrophy. 2008.