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Browsing by Author Dincsoy, Bir Firdevs
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| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2022 | A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation | Dincsoy, Bir Firdevs; Silan, Fatma; Velickovic, Jelena; Berkay, Akcan Mehmet; Ozdemir, Ozturk | Article | 23M23 |