Xp21 contiguous gene deletion syndrome: diagnosis, treatment, and a review of the literature on a rare genetic disorder.png)
IF1.5
Singin, Berna; Donbaloglu, Zeynep; Cetiner, Ebru Barsal; Bedel, Aynur; Cetin, Kursat; Paksoy, Belgin Akcan; Kalkan, Tarkan; Akbas, Halide; Tuhan, Hale Unver; Parlak, Mesut
Share
Save Gonadoblastoma with Dysgerminoma in a Virilized Adolescent with Karyotype 46,XX: A Case Report and Review of the Literature
Kandemir, Tugce; Ozturan, Esin Karakilic; Dural, Ozlem; Aslanger, Ayca Dilruba; Balci, Elif Inan; Bayram, Aysel; Onder, Semen; Kardelen, Asli Derya; Yildiz, Melek; Poyrazoglu, Sukran; Bas, Firdevs; Darendeliler, Feyza
Share
Save A Rare Coexistence of Turner Syndrome and Mycosis Fungoides: A Case Report
Demirel, Ozge Bayrak; Karakilic-Ozturan, Esin; Atci, Tugba; Sari, Sule Ozturk; Baykal, Can; Kardelen, Asli Derya; Yildiz, Melek; Poyrazoglu, Sukran; Bas, Firdevs; Darendeliler, Feyza
Share
Save A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism due to a Novel Homozygous Variant in the SCNN1B Gene
Singin, Berna; Donbaloglu, Zeynep; Cetiner, Ebru Barsal; Cetin, Kursat; Zarif, Nurten Ozkan; Celik, Kiymet; Mihci, Ercan; Clark, Ozden Altiok; Tuhan, Hale; Parlak, Mesut
Share
Save