KM
Karaoglan, Murat
3 yayın · 9 atıf · 2024–2025
Yayın
3
Atıf
9
Yıllar
2
Yayınlar
| Başlık | Yıl | Tip | Atıf |
|---|---|---|---|
|
A Little Known but Very Common Phenotype in Patients with Severe Congenital Neutropenia due to HAX1 Deficiency: Premature Ovarian Insufficiency
|
2025 | Article | 1 |
|
A Little Known But Very Common Phenotype in Patients with Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Failure
|
2024 | Meeting Abstract | 0 |
|
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
|
2024 | Article | 8 |