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.
Citace podle Chicago (17th ed.)Shield, J., SE Flanagan, D. Mackay, L. Harries, P. Proks, C. Girard, F. Ashcroft, I. Temple, a S. Ellard. Mosaic Paternal Uniparental Isodisomy and an ABCC8 Gene Mutation in a Patient with Permanent Neonatal Diabetes and Hemihypertrophy. 2008.
Citace podle MLA (9th ed.)Shield, J., et al. Mosaic Paternal Uniparental Isodisomy and an ABCC8 Gene Mutation in a Patient with Permanent Neonatal Diabetes and Hemihypertrophy. 2008.
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