TÜRKYILMAZ, A. Et Al. 2022. Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS , vol.39 , 695-710.

TÜRKYILMAZ, A., ALAVANDA, C., Ates, E. A., GEÇKİNLİ, B. B., Polat, H., GÖKCÜ, M., ... Karakaya, T.(2022). Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS , vol.39, 695-710.

TÜRKYILMAZ, AYBERK Et Al. "Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency," JOURNAL OF ASSISTED REPRODUCTION AND GENETICS , vol.39, 695-710, 2022

TÜRKYILMAZ, AYBERK Et Al. "Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency." JOURNAL OF ASSISTED REPRODUCTION AND GENETICS , vol.39, pp.695-710, 2022

TÜRKYILMAZ, A. Et Al. (2022) . "Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency." JOURNAL OF ASSISTED REPRODUCTION AND GENETICS , vol.39, pp.695-710.

@article{article, author={AYBERK TÜRKYILMAZ Et Al. }, title={Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency}, journal={JOURNAL OF ASSISTED REPRODUCTION AND GENETICS}, year=2022, pages={695-710} }