Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations (2017)
- Authors:
- USP affiliated authors: JORGE, ALEXANDER AUGUSTO DE LIMA - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- DOI: 10.1111/cen.13430
- Subjects: HORMÔNIOS HIPOFISÁRIOS; SEQUENCIAMENTO GENÉTICO; BRASILEIROS; ESTUDOS DE COORTES; MUTAÇÃO GENÉTICA
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical endocrinology
- ISSN: 0300-0664
- Volume/Número/Paginação/Ano: v. 87, n. 6, p. 725-732, 2017
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
MADEIRA, Joao Lo e JORGE, Alexander Augusto de Lima e MENDONÇA, Berenice Bilharinho de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations. Clinical endocrinology, v. 87, n. 6, p. 725-732, 2017Tradução . . Disponível em: https://doi.org/10.1111/cen.13430. Acesso em: 13 fev. 2026. -
APA
Madeira, J. L., Jorge, A. A. de L., & Mendonça, B. B. de. (2017). Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations. Clinical endocrinology, 87( 6), 725-732. doi:10.1111/cen.13430 -
NLM
Madeira JL, Jorge AA de L, Mendonça BB de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations [Internet]. Clinical endocrinology. 2017 ; 87( 6): 725-732.[citado 2026 fev. 13 ] Available from: https://doi.org/10.1111/cen.13430 -
Vancouver
Madeira JL, Jorge AA de L, Mendonça BB de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations [Internet]. Clinical endocrinology. 2017 ; 87( 6): 725-732.[citado 2026 fev. 13 ] Available from: https://doi.org/10.1111/cen.13430 - Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes
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Informações sobre o DOI: 10.1111/cen.13430 (Fonte: oaDOI API)
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