Rittig, S., Robertson, G. L., Siggaard, C., Kovács, L., Gregersen, N., Nyborg, J., & Pedersen, E. B. (1996). Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus.

Rittig, S., G. L. Robertson, C. Siggaard, L. Kovács, N. Gregersen, J. Nyborg, a E. B. Pedersen. Identification of 13 New Mutations in the Vasopressin-neurophysin II Gene in 17 Kindreds With Familial Autosomal Dominant Neurohypophyseal Diabetes Insipidus. 1996.

Rittig, S., et al. Identification of 13 New Mutations in the Vasopressin-neurophysin II Gene in 17 Kindreds With Familial Autosomal Dominant Neurohypophyseal Diabetes Insipidus. 1996.