Kizilay, D. O. Et Al. 2024. A Little Known But Very Common Phenotype in Patients with Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Failure. HORMONE RESEARCH IN PAEDIATRICS , 306.

Kizilay, D. O., Karapinar, D. Y., Karadas, N., Karaoglan, M., Akbayram, S., Goksen, D., ... Gadashova, A.(2024). A Little Known But Very Common Phenotype in Patients with Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Failure. HORMONE RESEARCH IN PAEDIATRICS , 306.

Kizilay, Deniz Et Al. "A Little Known But Very Common Phenotype in Patients with Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Failure," HORMONE RESEARCH IN PAEDIATRICS , 306, 2024

Kizilay, Deniz O. Et Al. "A Little Known But Very Common Phenotype in Patients with Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Failure." HORMONE RESEARCH IN PAEDIATRICS , pp.306, 2024

Kizilay, D. O. Et Al. (2024) . "A Little Known But Very Common Phenotype in Patients with Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Failure." HORMONE RESEARCH IN PAEDIATRICS , p.306.

@article{article, author={Deniz Ozalp Kizilay Et Al. }, title={A Little Known But Very Common Phenotype in Patients with Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Failure}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2024, pages={306} }