The Fanconi Anemia Pathway of Genomic Maintenance

Fanconi anemia (FA), a recessive syndrome with both autosomal and X-linked inheritance, features diverse clinical symptoms, such as progressive bone marrow failure, hypersensitivity to DNA cross-linking agents, chromosomal instability and susceptibility to cancer. At least 12 genetic subtypes have b...

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Detalles Bibliográficos
Autores principales: Levitus, Marieke, Joenje, Hans, de Winter, Johan P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2006
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4617492/
https://www.ncbi.nlm.nih.gov/pubmed/16675878
http://dx.doi.org/10.1155/2006/974975

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4617492/
https://www.ncbi.nlm.nih.gov/pubmed/16675878
http://dx.doi.org/10.1155/2006/974975

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