1. Further delineation of familial polycystic ovary syndrome (PCOS) via whole‐exome sequencing: PCOS‐related rare FBN3 and FN1 gene variants are identified. Issue 5 (9th February 2022) Authors: Karakaya, Cengiz; Çil, Aylin Pelin; Bilguvar, Kaya; Çakir, Tunahan; Karalok, Mete Hakan; Karabacak, Recep Onur; Caglayan, Ahmet Okay Journal: Journal of obstetrics and gynaecology research Issue: Volume 48:Issue 5(2022) Page Start: 1202 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗