Frequency of CHEK2*1100delC in New York breast cancer cases and controls
BACKGROUND: The 1100delC CHEK2 allele has been associated with a 1.4–4.7 fold increased risk for breast cancer in women carrying this mutation. While the frequency of 1100delC was 1.1–1.4% in healthy Finnish controls, the frequency of this allele in a North American control population and in North A...
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| Publicado no: | BMC Med Genet |
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| Principais autores: | , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMC
2003
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC149355/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12529183/ https://ncbi.nlm.nih.govhttps://doi.org/10.1186/1471-2350-4-1 |
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