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Fanconi anemia pathway defects in inherited and sporadic cancers
Fanconi anemia (FA) is a recessive chromosomal instability syndrome. It is a hereditary disorder with defects in DNA repair characterized by progressive bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors. Bi-allelic gene mutations in FA...
Tallennettuna:
| Julkaisussa: | Transl Pediatr |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
AME Publishing Company
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4728841/ https://ncbi.nlm.nih.gov/pubmed/26835350 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2224-4336.2014.07.05 |
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