Browsing by Author Albuz, B.
Showing results 1 to 2 of 2
| Issue Date | Title | Author(s) |
|---|---|---|
| 2017 | Congenital central hypothyroidism caused by a novel thyroid-stimulating hormone-beta subunit gene mutation in two siblings | Özhan, Bayram ; Anlaş, Ö.B.; Sarıkepe, B.; Albuz, B.; Gündüz, Nur Semerci |
| 2020 | A novel nonsense mutation in CHST3 in a Turkish patient with spondyloepiphyseal dysplasia, Omani type | Albuz, B.; Çetin, Gökhan Ozan ; Özhan, Bayram ; Sarikepe, B.; Anlaş, Ö.; Öztürk, M.; Zeybek, S. |