Yazar "Kor, Yilmaz" için listeleme
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Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets
Guven, Ayla; Al-Rijjal, Roua A.; BinEssa, Huda A.; Dogan, Durmus; Kor, Yilmaz; Zou, Minjing; Kaya, Namik; Alenezi, Anwar F.; Hancili, Suna; Tarim, Omer; Baitei, Essa Y.; Kattan, Walaa E.; Meyer, Brian F.; Shi, Yufei (WILEY, 2017)ContextHypophosphataemic rickets (HR) is a group of rare hereditary renal phosphate wasting disorders caused by mutations in PHEX, FGF23, DMP1, ENPP1, CLCN5 or SLC34A3. ObjectiveTo investigate underlying genetic defects ... -
PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: A MULTICENTER STUDY FROM TURKEY
Abaci, Ayhan; Catli, Gonul; Kirbiyik, Ozgur; Sahin, Nursel M.; Abali, Zehra Y.; Unal, Edip; Siklar, Zeynep; Ucakturk, Eda M.; Ozen, Samim; Guran, Tulay; Kara, Cengiz; Yildiz, Melek; Eren, Erdal; Nalbantoglu, Ozlem; Guven, Ayla; Cayir, Atilla; Akbas, Emine D.; Kor, Yilmaz; Curek, Yusuf; Aycan, Zehra; Bas, Firdevs; Darcan, Sukran; Berberoglu, Merih (KARGER, 2017)…
