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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...
Gorde:
| Argitaratua izan da: | Cell Oncol |
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| Egile Nagusiak: | , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
IOS Press
2006
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| Gaiak: | |
| Sarrera elektronikoa: | 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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