Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: GENÓTIPOS (ANORMALIDADES), DIABETES INSÍPIDO (GENÉTICA), BRASILEIROS (GENÉTICA, SEQUENCIAMENTO GENÉTICO
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MELO, M. E. et al. A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 16 out. 2024.APA
Melo, M. E., Marui, S., Mendonca, B. B., & Knoepfelmacher, M. (2004). A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus. In Program and Abstracts. Lisboa: International Society of Endocrinology.NLM
Melo ME, Marui S, Mendonca BB, Knoepfelmacher M. A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus. Program and Abstracts. 2004 ;[citado 2024 out. 16 ]Vancouver
Melo ME, Marui S, Mendonca BB, Knoepfelmacher M. A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus. Program and Abstracts. 2004 ;[citado 2024 out. 16 ]