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Genetic Analysis of RASD1 as a Candidate Gene for Schizophrenia.
Durmaz CD, Karabulut HG, Saka MC, Sucularlı C, Gümüş Akay G, Atbaşoğlu C, Ilgın Ruhi H. Durmaz CD, et al. Among authors: ilgin ruhi h. Balkan Med J. 2022 Nov 7;39(6):422-428. doi: 10.4274/balkanmedj.galenos.2022.2022-5-90. Epub 2022 Oct 28. Balkan Med J. 2022. PMID: 36305088 Free PMC article.
Bilateral choanal atresia in an adult woman with pycnodysostosis.
Durmaz CD, Taş V, Kocaay P, Fitöz ÖS, Onay H, Beton S, Özkınay F, Ilgın Ruhi H. Durmaz CD, et al. Among authors: ilgin ruhi h. Congenit Anom (Kyoto). 2017 May;57(3):91-92. doi: 10.1111/cga.12204. Congenit Anom (Kyoto). 2017. PMID: 27933642 No abstract available.
Association Between N363S and BclI Polymorphisms of the Glucocorticoid Receptor Gene (NR3C1) and Glucocorticoid Side Effects During Childhood Acute Lymphoblastic Leukemia Treatment.
Kaymak Cihan M, Karabulut HG, Yürür Kutlay N, Ilgın Ruhi H, Tükün A, Olcay L. Kaymak Cihan M, et al. Among authors: ilgin ruhi h. Turk J Haematol. 2017 Jun 5;34(2):151-158. doi: 10.4274/tjh.2016.0253. Epub 2017 Feb 9. Turk J Haematol. 2017. PMID: 28179212 Free PMC article.
A novel TWIST1 gene mutation in a patient with Saethre-Chotzen syndrome.
Altiner Ş, Karabulut HG, Yararbaş K, Tükün A, Collet C, Kocaay P, Berberoğlu M, Ilgin Ruhi H. Altiner Ş, et al. Among authors: ilgin ruhi h. Clin Dysmorphol. 2017 Jul;26(3):175-178. doi: 10.1097/MCD.0000000000000162. Clin Dysmorphol. 2017. PMID: 27870659 No abstract available.
18 results