APA (7th ed.) Citation

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.

Chicago Style (17th ed.) Citation

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

MLA (9th ed.) Citation

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