KARAKAYA, C. Et Al. 2022. Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified. JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH , vol.48, no.5 , 1202-1211.

KARAKAYA, C., Cil, A. P., Bilguvar, K., ÇAKIR, T., Karalok, M. H., KARABACAK, R. O., ... ÇAĞLAYAN, A. O.(2022). Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified. JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH , vol.48, no.5, 1202-1211.

KARAKAYA, CENGİZ Et Al. "Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified," JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH , vol.48, no.5, 1202-1211, 2022

KARAKAYA, CENGİZ Et Al. "Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified." JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH , vol.48, no.5, pp.1202-1211, 2022

KARAKAYA, C. Et Al. (2022) . "Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified." JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH , vol.48, no.5, pp.1202-1211.

@article{article, author={CENGİZ KARAKAYA Et Al. }, title={Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified}, journal={JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH}, year=2022, pages={1202-1211} }