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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...

詳細記述

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書誌詳細
出版年:Cell Oncol
主要な著者: Levitus, Marieke, Joenje, Hans, de Winter, Johan P.
フォーマット: Artigo
言語:Inglês
出版事項: IOS Press 2006
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4617492/
https://ncbi.nlm.nih.gov/pubmed/16675878
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2006/974975
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