Evidence of linkage to chromosomes 10p15.3–p15.1, 14q24.3–q31.1 and 9q33.3–q34.3 in non-syndromic colorectal cancer families

Up to 25% of colorectal cancer (CRC) may be caused by inherited genetic variants that have yet to be identified. Previous genome-wide linkage studies (GWLSs) have identified a new loci postulated to contain novel CRC risk genes amongst affected families carrying no identifiable mutations in any of t...

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Detalhes bibliográficos
Main Authors: Saunders, Ian W, Ross, Jason, Macrae, Finlay, Young, Graeme P, Blanco, Ignacio, Brohede, Jesper, Brown, Glenn, Brookes, Diana, Lockett, Trevor, Molloy, Peter L, Moreno, Victor, Capella, Gabriel, Hannan, Garry N
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3234517/
https://ncbi.nlm.nih.gov/pubmed/21829229
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2011.149
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