N.F Topbas Selcuki

No ORCID on file · 1 paper in corpus

article 2022

P-301 Exome sequencing reveals novel candidate variants for endometriosis and endometrial serous adenocarcinoma in a single family having multiple affected members

·doi:10.1093/humrep/deac107.287

Abstract Study question Could genetic evaluation of a family, having multiple affected members with endometriosis, contribute to identifying novel rare variants for the missing heritability of the disease? Summary answer Two novel genetic v…