Evolving combined pituitary hormone deficiency (CPHD) and ectopic posterior pituitary (EPP) is associated with a novel homozygous missense mutation (I26T) in the HESX1 repressor domain (2002)
- Authors:
- Autor USP: MENDONCA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: HORMÔNIOS HIPOFISÁRIOS (DEFICIÊNCIA); ENDOCRINOPATIAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Hormone Research
- ISSN: 0301-0163
- Volume/Número/Paginação/Ano: v. 58, supp. 2, p. 95, res. P2-333, 2002
- Conference titles: Annual Meeting of the European Society for Paediatric Endocrinology (ESPE
-
ABNT
CARVALHO, L. R. et al. Evolving combined pituitary hormone deficiency (CPHD) and ectopic posterior pituitary (EPP) is associated with a novel homozygous missense mutation (I26T) in the HESX1 repressor domain. Hormone Research. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 abr. 2024. , 2002 -
APA
Carvalho, L. R., Woods, K. S., Zamparini, A. L., Mendonça, B. B., Brickman, J. M., Arnhold, I. J., & Dattani, M. T. (2002). Evolving combined pituitary hormone deficiency (CPHD) and ectopic posterior pituitary (EPP) is associated with a novel homozygous missense mutation (I26T) in the HESX1 repressor domain. Hormone Research. Basel: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Carvalho LR, Woods KS, Zamparini AL, Mendonça BB, Brickman JM, Arnhold IJ, Dattani MT. Evolving combined pituitary hormone deficiency (CPHD) and ectopic posterior pituitary (EPP) is associated with a novel homozygous missense mutation (I26T) in the HESX1 repressor domain. Hormone Research. 2002 ; 58 95.[citado 2024 abr. 24 ] -
Vancouver
Carvalho LR, Woods KS, Zamparini AL, Mendonça BB, Brickman JM, Arnhold IJ, Dattani MT. Evolving combined pituitary hormone deficiency (CPHD) and ectopic posterior pituitary (EPP) is associated with a novel homozygous missense mutation (I26T) in the HESX1 repressor domain. Hormone Research. 2002 ; 58 95.[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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