Combined iPLEX and TaqMan Assays to Screen for 45 Common Mutations in Lynch Syndrome and FAP Patients

Mutations of genes associated with the mismatch repair mechanism and mutations of the APC gene are the most frequent causes of hereditary colorectal cancer. An iPLEX test combined with TaqMan genotyping assays was therefore developed to identify common recurrent mutations of those genes in the Polis...

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Detalhes bibliográficos
Main Authors: Dymerska, Dagmara, Serrano-Fernández, Pablo, Suchy, Janina, Pławski, Andrzej, Słomski, Ryszard, Kąklewski, Krzysztof, Scott, Rodney J., Gronwald, Jacek, Kładny, Józef, Byrski, Tomasz, Huzarski, Tomasz, Lubiński, Jan, Kurzawski, Grzegorz
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2010
Assuntos:
Regular Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2797722/
https://ncbi.nlm.nih.gov/pubmed/20007843
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/jmoldx.2010.090063
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