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HCAD, closing the gap between breakpoints and genes

Recurrent chromosome aberrations are an important resource when associating human pathologies to specific genes. However, for technical reasons a large number of chromosome breakpoints are defined only at the level of cytobands and many of the genes involved remain unidentified. We developed a web-b...

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Detalhes bibliográficos
Main Authors: Hoffmann, Robert, Dopazo, Joaquin, Cigudosa, Juan C., Valencia, Alfonso
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2005
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC540015/
https://ncbi.nlm.nih.gov/pubmed/15608250
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gki061
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