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Sequencing Complex Diseases With HapMap

Determining the patterns of DNA sequence variation in the human genome is a useful first step toward identifying the genetic basis of a common disease. A haplotype map (HapMap), aimed at describing these variation patterns across the entire genome, has been recently developed by the International Ha...

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Detalhes bibliográficos
Main Authors: Liu, Tian, Johnson, Julie A., Casella, George, Wu, Rongling
Formato: Artigo
Idioma:Inglês
Publicado em: Genetics Society of America 2004
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1448119/
https://ncbi.nlm.nih.gov/pubmed/15454560
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.104.029603
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