Skip to Main Content

Paper Details

FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation.
Hum Mol Genet
91
2009
BC, DNase I hypersensitive sites, FGFR2, FGFR2 variants, SNP, SNP rs2981578, SNPs, breast cancer, candidate-causal SNPs, chromatin, invasive BC, rs2981578, susceptibility variants, which, SN, women
Author NameAffiliation
Miriam S UdlerUniversity of Cambridge
  • 1 - 1

Datasets

Release 1.2