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POU6F2 mutation in humans with pubertal failure alters GnRH transcript expression.
Cho HJ, Gurbuz F, Stamou M, Kotan LD, Farmer SM, Can S, Tompkins MF, Mammadova J, Altincik SA, Gokce C, Catli G, Bugrul F, Bartlett K, Turan I, Balasubramanian R, Yuksel B, Seminara SB, Wray S, Topaloglu AK. Cho HJ, et al. Among authors: yuksel b. Front Endocrinol (Lausanne). 2023 Aug 1;14:1203542. doi: 10.3389/fendo.2023.1203542. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37600690 Free PMC article.
A novel homozygous nonsense NDNF variant in Kallmann syndrome.
Kotan LD, Yildiz M, Turan I, Celiloglu C, Yuksel B, Topaloglu AK. Kotan LD, et al. Among authors: yuksel b. Am J Med Genet A. 2023 Mar;191(3):831-834. doi: 10.1002/ajmg.a.63066. Epub 2022 Dec 1. Am J Med Genet A. 2023. PMID: 36454653
Different Clinical Effects of Ectodermal Dysplasias in Four Generations.
Demirhan O, Yüksel B, Yilmaz S, Cetinel N. Demirhan O, et al. Among authors: yuksel b. Actas Dermosifiliogr. 2023 Nov-Dec;114(10):T918-T920. doi: 10.1016/j.ad.2023.09.007. Epub 2023 Sep 15. Actas Dermosifiliogr. 2023. PMID: 37716501 Free article. English, Spanish. No abstract available.
Different Clinical Effects of Ectodermal Dysplasias in Four Generations.
Demirhan O, Yüksel B, Yilmaz S, Cetinel N. Demirhan O, et al. Among authors: yuksel b. Actas Dermosifiliogr. 2023 Nov-Dec;114(10):918-920. doi: 10.1016/j.ad.2022.11.017. Epub 2023 Jun 3. Actas Dermosifiliogr. 2023. PMID: 37276991 Free article. English, Spanish. No abstract available.
387 results