Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified.


Karakaya C., Çil A. P., Bilguvar K., Çakir T., Karalok M. H., Karabacak R. O., ...More

The journal of obstetrics and gynaecology research, 2022 (SCI-Expanded) identifier