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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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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2008
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2556683/ https://ncbi.nlm.nih.gov/pubmed/18786261 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2407-8-257 |
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