APA-ийн эшлэл(7 дахь хэвлэлт)

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.

Чикаго-гийн эшлэл (17 дахь хэвлэлт)

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

MLA -ийн эшлэл (9 дэх хэвлэлт)

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