Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families

BACKGROUND: The dominantly inherited condition familial adenomatous polyposis (FAP) is caused by germline mutations in the APC gene. Finding the causative mutations has great implications for the families. Correlating the genotypes to the phenotypes could help to improve the diagnosis and follow-up...

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Detalhes bibliográficos
Main Authors: Kanter-Smoler, Gunilla, Fritzell, Kaisa, Rohlin, Anna, Engwall, Yvonne, Hallberg, Birgitta, Bergman, Annika, Meuller, Johan, Grönberg, Henrik, Karlsson, Per, Björk, Jan, Nordling, Margareta
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2008
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2386495/
https://ncbi.nlm.nih.gov/pubmed/18433509
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1741-7015-6-10
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