Shelling AN

No ORCID on file · 2 papers in corpus · active 2000-2024
2024
Human genetics ·doi:10.1007/s00439-024-02707-9

Known risk loci for endometrial cancer explain approximately one third of familial endometrial cancer. However, the association of germline copy number variants (CNVs) with endometrial cancer risk remains relatively unknown. We conducted a …

2000
Journal of medical genetics ·doi:10.1136/jmg.37.5.e2