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.