Molecular analysis of hemophilia b in brazilian patients (1993)
- Autor:
- Autor USP: FIGUEIREDO, MAURO SILVERIO - FMRP
- Unidade: FMRP
- Assunto: MEDICINA INTERNA
- Language: Inglês
- Imprenta:
- Publisher place: Ribeirao Preto
- Date published: 1993
- Source:
- Título do periódico: Brazilian Journal of Medical and Biological Research
- Volume/Número/Paginação/Ano: v.26, n.9 , p.919-31, set. 1993
-
ABNT
FIGUEIREDO, Mauro Silvério. Molecular analysis of hemophilia b in brazilian patients. Brazilian Journal of Medical and Biological Research, v. 26, n. 9 , p. 919-31, 1993Tradução . . Acesso em: 04 maio 2024. -
APA
Figueiredo, M. S. (1993). Molecular analysis of hemophilia b in brazilian patients. Brazilian Journal of Medical and Biological Research, 26( 9 ), 919-31. -
NLM
Figueiredo MS. Molecular analysis of hemophilia b in brazilian patients. Brazilian Journal of Medical and Biological Research. 1993 ;26( 9 ): 919-31.[citado 2024 maio 04 ] -
Vancouver
Figueiredo MS. Molecular analysis of hemophilia b in brazilian patients. Brazilian Journal of Medical and Biological Research. 1993 ;26( 9 ): 919-31.[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
- Haemophilia b liverpol: a new british family with mild haemophilia b associated with a -6 g to a mutation in the factor ix promotor
- 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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