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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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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2005
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| Matèries: | |
| Accés en línia: | 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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