A novel homozygous mis-sense mutation (I26T) in the repressor domain of the transcription factor HESX1 is associadet with evolving combined pituitary hormone deficiency (CPHD) and ectopic posterior lobe (PL) in the absence of forebrain defect (2002)
- Autores:
- Autores USP: MENDONCA, BERENICE BILHARINHO DE - FM ; ARNHOLD, IVO JORGE PRADO - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Idioma: Inglês
- Imprenta:
- Local: San Francisco
- Data de publicação: 2002
- Fonte:
- Título do periódico: Resumos
- Nome do evento: Annual Metting the Endrocrine Society's
-
ABNT
CARVALHO, Luciani R. et al. A novel homozygous mis-sense mutation (I26T) in the repressor domain of the transcription factor HESX1 is associadet with evolving combined pituitary hormone deficiency (CPHD) and ectopic posterior lobe (PL) in the absence of forebrain defect. 2002, Anais.. San Francisco: Faculdade de Medicina, Universidade de São Paulo, 2002. . Acesso em: 16 abr. 2024. -
APA
Carvalho, L. R., Woods, K. S., Zamparini, A. L., Mendonça, B. B. de, Brickman, J. M., Arnhold, I. J. P., & Dattani, M. T. (2002). A novel homozygous mis-sense mutation (I26T) in the repressor domain of the transcription factor HESX1 is associadet with evolving combined pituitary hormone deficiency (CPHD) and ectopic posterior lobe (PL) in the absence of forebrain defect. In Resumos. San Francisco: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Carvalho LR, Woods KS, Zamparini AL, Mendonça BB de, Brickman JM, Arnhold IJP, Dattani MT. A novel homozygous mis-sense mutation (I26T) in the repressor domain of the transcription factor HESX1 is associadet with evolving combined pituitary hormone deficiency (CPHD) and ectopic posterior lobe (PL) in the absence of forebrain defect. Resumos. 2002 ;[citado 2024 abr. 16 ] -
Vancouver
Carvalho LR, Woods KS, Zamparini AL, Mendonça BB de, Brickman JM, Arnhold IJP, Dattani MT. A novel homozygous mis-sense mutation (I26T) in the repressor domain of the transcription factor HESX1 is associadet with evolving combined pituitary hormone deficiency (CPHD) and ectopic posterior lobe (PL) in the absence of forebrain defect. Resumos. 2002 ;[citado 2024 abr. 16 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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