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Copy number variation at the breakpoint region of isochromosome 17q
Isochromosome 17q, or i(17q), is one of the most frequent nonrandom changes occurring in human neoplasia. Most of the i(17q) breakpoints cluster within a ∼240-kb interval located in the Smith-Magenis syndrome common deletion region in 17p11.2. The breakpoint cluster region is characterized by a comp...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2008
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2577857/ https://ncbi.nlm.nih.gov/pubmed/18714090 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.080697.108 |
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