A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus (2004)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: GENÓTIPOS (ANORMALIDADES); DIABETES INSÍPIDO (GENÉTICA); BRASILEIROS (GENÉTICA; SEQUENCIAMENTO GENÉTICO
- Language: Inglês
- Imprenta:
- Publisher: International Society of Endocrinology
- Publisher place: Lisboa
- Date published: 2004
- Source:
- Título do periódico: Program and Abstracts
- Conference titles: International Congress of Endocrinology
-
ABNT
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: 24 abr. 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 abr. 24 ] -
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 abr. 24 ] - Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
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