Haemophilia b liverpol: a new british family with mild haemophilia b associated with a -6 g to a mutation in the factor ix promotor (1993)
- Authors:
- Autor USP: FIGUEIREDO, MAURO SILVERIO - FMRP
- Unidade: FMRP
- Assunto: HEMATOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: British Journal of Haematology
- Volume/Número/Paginação/Ano: v.85, n.1 , p.188-90, 1993
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ABNT
STOWEL, K M et al. Haemophilia b liverpol: a new british family with mild haemophilia b associated with a -6 g to a mutation in the factor ix promotor. British Journal of Haematology, v. 85, n. 1 , p. 188-90, 1993Tradução . . Acesso em: 04 maio 2024. -
APA
Stowel, K. M., Figueiredo, M. S., Brownlee, G. G., Jones, P., & Bolton Maggs, P. H. B. (1993). Haemophilia b liverpol: a new british family with mild haemophilia b associated with a -6 g to a mutation in the factor ix promotor. British Journal of Haematology, 85( 1 ), 188-90. -
NLM
Stowel KM, Figueiredo MS, Brownlee GG, Jones P, Bolton Maggs PHB. Haemophilia b liverpol: a new british family with mild haemophilia b associated with a -6 g to a mutation in the factor ix promotor. British Journal of Haematology. 1993 ;85( 1 ): 188-90.[citado 2024 maio 04 ] -
Vancouver
Stowel KM, Figueiredo MS, Brownlee GG, Jones P, Bolton Maggs PHB. Haemophilia b liverpol: a new british family with mild haemophilia b associated with a -6 g to a mutation in the factor ix promotor. British Journal of Haematology. 1993 ;85( 1 ): 188-90.[citado 2024 maio 04 ] - Genes dos fatores viii e ix da coagulação . Hemofilias
- Novel and recurrent mutations of factor ix gene in brazilian hemophilia b patients
- Location and rapid analysis of the intragenic bam hi polymorphic site of the factor ix gene
- Polimorfismos de restricao do gene do fator viii em populacao negra brasileira
- Mutacao - 601t-c da regiao promotora do gene do fator viii ao determinar reducao de sua atividade funcional
- Genes dos fatores viii e ix da coagulacao: mutacoes, polimorfismos e controle da expressao genica
- Transcription factor and cis-acting elements involved in the promoter activity of the human factor viii gene
- Molecular analysis of hemophilia b in brazilian patients
- Moderation of hemophilia a phenotype by the factor v r506q mutation
- High frequence of the - 6g to a factor ix promoter mutation is the result of both a founder effect and recurrent mutation at a crg dinucleotide
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