Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer
Familial clustering studies indicate that breast cancer risk has a substantial genetic component 1 , 2 , 3 . To identify new breast cancer risk variants, we genotyped approximately 300,000 SNPs in 1,600 Icelandic individuals with breast cancer and 11,563 controls using the Illumina Hap300 platform....
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Veröffentlicht in: | Nature genetics 2007-07, Vol.39 (7), p.865-869 |
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