Elevated sister chromatid exchange phenotype of Bloom syndrome cells is complemented by human chromosome 15.
Bloom syndrome (BSx) is a rare autosomal-recessive chromosome-instability disorder manifested by a constellation of clinical features including a significant predisposition to early onset of neoplasia. BSx cells display cytogenetic abnormalities, the pathognomonic feature being an increased rate of...
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| 發表在: | Proc Natl Acad Sci U S A |
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| Principais autores: | , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
National Academy of Sciences
1992
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC49836/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1518822/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.89.17.7968 |
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