Heidi Miedl
ORCID: 0000-0003-4575-639X
· 1 paper in corpus
In this focused genetic case-control study, we analyzed two functional single-nucleotide variants (SNVs) associated with breast cancer risk (rs2046210, rs9383590) and one risk SNV for an implantation defect and infertility (rs9340799) for t…