Location and rapid analysis of the intragenic bam hi polymorphic site of the factor ix gene (1994)
- Autor:
- Autor USP: FIGUEIREDO, MAURO SILVERIO - FMRP
- Unidade: FMRP
- Assunto: GENÉTICA
- Language: Inglês
- Imprenta:
- Publisher place: Ribeirao Preto
- Date published: 1994
- Source:
- Título do periódico: Brazilian Journal of Medical and Biological Research
- Volume/Número/Paginação/Ano: v.27, p.1117-21, 1994
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ABNT
FIGUEIREDO, Mauro Silvério. Location and rapid analysis of the intragenic bam hi polymorphic site of the factor ix gene. Brazilian Journal of Medical and Biological Research, v. 27, p. 1117-21, 1994Tradução . . Acesso em: 18 abr. 2024. -
APA
Figueiredo, M. S. (1994). Location and rapid analysis of the intragenic bam hi polymorphic site of the factor ix gene. Brazilian Journal of Medical and Biological Research, 27, 1117-21. -
NLM
Figueiredo MS. Location and rapid analysis of the intragenic bam hi polymorphic site of the factor ix gene. Brazilian Journal of Medical and Biological Research. 1994 ;27 1117-21.[citado 2024 abr. 18 ] -
Vancouver
Figueiredo MS. Location and rapid analysis of the intragenic bam hi polymorphic site of the factor ix gene. Brazilian Journal of Medical and Biological Research. 1994 ;27 1117-21.[citado 2024 abr. 18 ] - Genes dos fatores viii e ix da coagulação . Hemofilias
- Novel and recurrent mutations of factor ix gene in brazilian hemophilia b patients
- 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
- 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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