Heidi Miedl

ORCID: 0000-0003-4575-639X · 1 paper in corpus
other 2024
Biomedicines ·doi:10.3390/biomedicines12081657

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…