Evidence for at least eight Fanconi anemia genes.

Fanconi anemia (FA) is an autosomal recessive chromosomal breakage disorder with diverse clinical symptoms including progressive bone marrow failure and increased cancer risk. FA cells are hypersensitive to crosslinking agents, which has been exploited to assess genetic heterogeneity through complem...

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Detalhes bibliográficos
Main Authors: Joenje, H, Oostra, A B, Wijker, M, di Summa, F M, van Berkel, C G, Rooimans, M A, Ebell, W, van Weel, M, Pronk, J C, Buchwald, M, Arwert, F
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715980/
https://ncbi.nlm.nih.gov/pubmed/9382107
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