APA

Repaske D. R., Summar M. L., Krishnamani M. R., Gültekin E. K., Arriazu M. C., Roubicek M. E., Blanco M., Isaac G. B. & Phillips J. A. (19961211). Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidus. : The Journal of clinical endocrinology and metabolism.

Chicago

Repaske D R, Summar M L, Krishnamani M R, Gültekin E K, Arriazu M C, Roubicek M E, Blanco M, Isaac G B and Phillips J A. 19961211. Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidus. : The Journal of clinical endocrinology and metabolism.

Harvard

Repaske D. R., Summar M. L., Krishnamani M. R., Gültekin E. K., Arriazu M. C., Roubicek M. E., Blanco M., Isaac G. B. and Phillips J. A. (19961211). Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidus. : The Journal of clinical endocrinology and metabolism.

MLA

Repaske D R, Summar M L, Krishnamani M R, Gültekin E K, Arriazu M C, Roubicek M E, Blanco M, Isaac G B and Phillips J A. Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidus. : The Journal of clinical endocrinology and metabolism. 19961211.