Eren, S. Et Al. 2024. A Rare Cause of Primary Ovarian Insufficiency: Novel Homozygous c.2120G>C(p.Arg707Pro) Pathogenic Variant in the MCM8 Gene. HORMONE RESEARCH IN PAEDIATRICS , 460-461.

Eren, S., TÜRKYILMAZ, A., Ozdemir, M., & Ucar, A., (2024). A Rare Cause of Primary Ovarian Insufficiency: Novel Homozygous c.2120G>C(p.Arg707Pro) Pathogenic Variant in the MCM8 Gene. HORMONE RESEARCH IN PAEDIATRICS , 460-461.

Eren, Simge Et Al. "A Rare Cause of Primary Ovarian Insufficiency: Novel Homozygous c.2120G>C(p.Arg707Pro) Pathogenic Variant in the MCM8 Gene," HORMONE RESEARCH IN PAEDIATRICS , 460-461, 2024

Eren, Simge Et Al. "A Rare Cause of Primary Ovarian Insufficiency: Novel Homozygous c.2120G>C(p.Arg707Pro) Pathogenic Variant in the MCM8 Gene." HORMONE RESEARCH IN PAEDIATRICS , pp.460-461, 2024

Eren, S. Et Al. (2024) . "A Rare Cause of Primary Ovarian Insufficiency: Novel Homozygous c.2120G>C(p.Arg707Pro) Pathogenic Variant in the MCM8 Gene." HORMONE RESEARCH IN PAEDIATRICS , pp.460-461.

@article{article, author={Simge Eren Et Al. }, title={A Rare Cause of Primary Ovarian Insufficiency: Novel Homozygous c.2120G>C(p.Arg707Pro) Pathogenic Variant in the MCM8 Gene}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2024, pages={460-461} }