Fonte: Program and Abstracts. Nome do evento: Annual Meeting of the Endocrine Society. Unidade: FMRP
Assunto: ENDOCRINOLOGIA
ABNT
ELIAS, P. C. L. et al. A novel mutation in the vasopressin-neurofisin II gene (Ala68Pro) associated with familial autosomal dominant neurohypophyseal diabetes insipidus. 2002, Anais.. San Francisco: Endocrine Society, 2002. . Acesso em: 18 nov. 2024.APA
Elias, P. C. L., Elias, L. L. L. K., Torres, N., Moreira, A. C., Antunes-Rodrigues, J., & Castro, M. de. (2002). A novel mutation in the vasopressin-neurofisin II gene (Ala68Pro) associated with familial autosomal dominant neurohypophyseal diabetes insipidus. In Program and Abstracts. San Francisco: Endocrine Society.NLM
Elias PCL, Elias LLLK, Torres N, Moreira AC, Antunes-Rodrigues J, Castro M de. A novel mutation in the vasopressin-neurofisin II gene (Ala68Pro) associated with familial autosomal dominant neurohypophyseal diabetes insipidus. Program and Abstracts. 2002 ;[citado 2024 nov. 18 ]Vancouver
Elias PCL, Elias LLLK, Torres N, Moreira AC, Antunes-Rodrigues J, Castro M de. A novel mutation in the vasopressin-neurofisin II gene (Ala68Pro) associated with familial autosomal dominant neurohypophyseal diabetes insipidus. Program and Abstracts. 2002 ;[citado 2024 nov. 18 ]