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Artigo de periodico
A homozygous mutation in HESX1 is associated with evolving hyppopituitarism due to impaired repressor-corepressor interaction (2003)
Carvalho, Luciani R.; Woods, Kathryn S.; Mendonça, Berenice B.; Marcal, Nathalhie; Zamparini, Andrea L.; Stifani, Stefano; Brickman, Joshua M.; Arnhold, Ivo J. P.; Dattani, Mehul T.
Source: Journal of Clinical Investigation. Unidade: FM
Subject: GLÂNDULA PITUITÁRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Luciani R.; WOODS, Kathryn S.; MENDONÇA, Berenice B.; et al. A homozygous mutation in HESX1 is associated with evolving hyppopituitarism due to impaired repressor-corepressor interaction. Journal of Clinical Investigation, Massachussetts, v. 112, n. 8, p. 1192-1201, 2003. DOI: 10.1172/jci18589.
APA
Carvalho, L. R., Woods, K. S., Mendonça, B. B., Marcal, N., Zamparini, A. L., Stifani, S., et al. (2003). A homozygous mutation in HESX1 is associated with evolving hyppopituitarism due to impaired repressor-corepressor interaction. Journal of Clinical Investigation, 112( 8), 1192-1201. doi:10.1172/jci18589
NLM
Carvalho LR, Woods KS, Mendonça BB, Marcal N, Zamparini AL, Stifani S, Brickman JM, Arnhold IJP, Dattani MT. A homozygous mutation in HESX1 is associated with evolving hyppopituitarism due to impaired repressor-corepressor interaction. Journal of Clinical Investigation. 2003 ; 112( 8): 1192-1201.
Vancouver
Carvalho LR, Woods KS, Mendonça BB, Marcal N, Zamparini AL, Stifani S, Brickman JM, Arnhold IJP, Dattani MT. A homozygous mutation in HESX1 is associated with evolving hyppopituitarism due to impaired repressor-corepressor interaction. Journal of Clinical Investigation. 2003 ; 112( 8): 1192-1201.
Trabalho de evento-resumo
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)
Carvalho, Luciani R.; Woods, Kathryn S.; Zamparini, Andrea L.; Mendonça, Berenice Bilharinho de; Brickman, Joshua M.; Arnhold, Ivo Jorge Prado; Dattani, Mehul T.
Source: Resumos. Conference title: Annual Metting the Endrocrine Society's. Unidade: FM
Subject: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Luciani R.; WOODS, Kathryn S.; ZAMPARINI, Andrea L.; 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. Anais.. San Francisco: [s.n.], 2002.
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.
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 ;
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 ;

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