APA

Melo M. E. d., Marui S., Brito V. N. d., Mancini M. C., Mendonca B. B. & Knoepfelmacher M. (20091007). Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family. : Arquivos brasileiros de endocrinologia e metabologia.

Chicago

Melo Maria Edna de, Marui Suemi, Brito Vinícius Nahime de, Mancini Marcio Corrêa, Mendonca Berenice B and Knoepfelmacher Mirta. 20091007. Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family. : Arquivos brasileiros de endocrinologia e metabologia.

Harvard

Melo M. E. d., Marui S., Brito V. N. d., Mancini M. C., Mendonca B. B. and Knoepfelmacher M. (20091007). Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family. : Arquivos brasileiros de endocrinologia e metabologia.

MLA

Melo Maria Edna de, Marui Suemi, Brito Vinícius Nahime de, Mancini Marcio Corrêa, Mendonca Berenice B and Knoepfelmacher Mirta. Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family. : Arquivos brasileiros de endocrinologia e metabologia. 20091007.