Cancer incidence in relatives of British Fanconi Anaemia patients

BACKGROUND: Fanconi anemia (FA) is an autosomal recessive DNA repair disorder with affected individuals having a high risk of developing acute myeloid leukaemia and certain solid tumours. Thirteen complementation groups have been identified and the genes for all of these are known (FANCA, B, C, D1/B...

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Detalles Bibliográficos
Autores principales: Tischkowitz, Marc, Easton, Douglas F, Ball, Jan, Hodgson, Shirley V, Mathew, Christopher G
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2556683/
https://www.ncbi.nlm.nih.gov/pubmed/18786261
http://dx.doi.org/10.1186/1471-2407-8-257

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2556683/
https://www.ncbi.nlm.nih.gov/pubmed/18786261
http://dx.doi.org/10.1186/1471-2407-8-257

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