APA aipamena

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 aipamena

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 aipamena

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