Wordt geladen...
The molecular mechanism underlying formation of deletions in Fanconi anemia cells may involve a site-specific recombination.
Spontaneous and induced chromosomal breakage is an important cellular feature of Fanconi anemia (FA), an inherited DNA repair disorder characterized by progressive bone marrow failure, developmental abnormalities, and predisposition to leukemia. We have previously reported that in comparison to norm...
Bewaard in:
| Hoofdauteurs: | , , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
1995
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC42714/ https://ncbi.nlm.nih.gov/pubmed/7846061 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|