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High-throughput genotyping of a common deletion polymorphism disrupting the TRY6 gene and its association with breast cancer risk
BACKGROUND: Copy number polymorphisms caused by genomic rearrangements like deletions, make a significant contribution to the genomic differences between two individuals and may add to disease predisposition. Therefore, genotyping of such deletion polymorphisms in case-control studies could give imp...
| Autores principales: | , , , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2007
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1925117/ https://www.ncbi.nlm.nih.gov/pubmed/17598925 http://dx.doi.org/10.1186/1471-2156-8-41 |