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PLXNB1 mutations in the etiology of idiopathic hypogonadotropic hypogonadism.
Welch BA, Cho HJ, Ucakturk SA, Farmer SM, Cetinkaya S, Abaci A, Akkus G, Simsek E, Kotan LD, Turan I, Gurbuz F, Yuksel B, Wray S, Topaloglu AK. Welch BA, et al. Among authors: ucakturk sa. J Neuroendocrinol. 2022 Apr;34(4):e13103. doi: 10.1111/jne.13103. Epub 2022 Feb 16. J Neuroendocrinol. 2022. PMID: 35170806
A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome.
Mengen E, Kotan LD, Ucakturk SA, Topaloglu AK, Yuksel B. Mengen E, et al. Among authors: ucakturk sa. J Coll Physicians Surg Pak. 2018 May;28(5):403-405. doi: 10.29271/jcpsp.2018.05.403. J Coll Physicians Surg Pak. 2018. PMID: 29690975
Effects of 5-Hydroxymethylfurfural on Pubertal Development of Female Wistar Rats.
Elmaoğulları S, Kadan E, Anadol E, Gökçeoğlu A, Çetinkaya S, Yarım GF, Uçaktürk SA, Aycan Z. Elmaoğulları S, et al. Among authors: ucakturk sa. J Clin Res Pediatr Endocrinol. 2020 Mar 19;12(1):79-85. doi: 10.4274/jcrpe.galenos.2019.2019.0080. Epub 2019 Sep 2. J Clin Res Pediatr Endocrinol. 2020. PMID: 31475510 Free PMC article.
26 results