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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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Bibliografische Detailangaben
Veröffentlicht in:BMC Med Genet
Hauptverfasser: Offit, Kenneth, Pierce, Heather, Kirchhoff, Tomas, Kolachana, Prema, Rapaport, Beth, Gregersen, Peter, Johnson, Steven, Yossepowitch, Orit, Huang, Helen, Satagopan, Jaya, Robson, Mark, Scheuer, Lauren, Nafa, Khedoudja, Ellis, Nathan
Format: Artigo
Sprache:Inglês
Veröffentlicht: BMC 2003
Schlagworte:
Online-Zugang: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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