D. Karaer
Karaer, Derya.
Publications
(Articles)
Results 1-6 of 6 (Search time: 0.013 seconds).
Issue Date | Title | Author(s) | |
---|---|---|---|
1 | 2024 | A case report of Hennekam syndrome with a mutation in the CCBE1 gene | Durak, T. ; Karaer, D. ; Karaer, K. |
2 | 2023 | Evaluation of the frequency of MEFV gene variants in patients with a pre-diagnosis of Familial Mediterranean Fever (FMF) in southeast Türkiye | Karaer, Derya ; Şahinoğlu, Bahtiyar; Gürler, Abdullah İhsan; Karaer, Kadri |
3 | 2021 | İnfertil erkek hastalarda karyotip analizi ve Y kromozom mikrodelesyon analiz sonuçları | Karaer, Derya ; Şahinoğlu, Bahtiyar; Gürler, Abdullah İhsan; Kadri Karaer |
4 | 2023 | The Molecular Spectrum of Beta Thalassemia Mutations in Southeastern, Turkey | Karaer, Derya ; Şahinoğlu, Bahtiyar; Şahinoğlu, Esra Pekpak; Gürler, Abdullah I.; Kirat, Emre; Karaer, Kadri |
5 | 2022 | Neurodevelopmental disorder with microcephaly, ataxia, and seizures syndrome: expansion of the clinical spectrum | Karaer K. ; Karaer D. ; Yüksel Z.; Işikay S. |
6 | 2022 | Two novel variants in SCARF2 gene underlie van den Ende-Gupta syndrome | Karaer, Derya ; Karaer, Kadri |
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