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Autor:
Esra niz P. De Cakir, Eda Mengen, Olcay Evliyaoğlu, Paolo Giacobini, A. Kemal Topaloglu, Ihsan Turan, Gaspard Delpouve, Gamze Akkus, Feyza Darendeliler, Aysegul Yuksel, Asli rya De Kardelen, Fatih Gurbuz, Aydilek Dagdeviren Cakir, Sebahat Yılmaz Ağladıoğlu, Semine Özdemir Dilek, Bilgin Yüksel, Gaetan Ternier, Bahar Ozcabi, Hamdi Cihan Emeksiz, Emregul Isik, Leman Damla Kotan
Publikováno v:
Genet Med
Genetics in Medicine
Genetics in Medicine
Purpose Idiopathic hypogonadotropic hypogonadism (IHH) is characterized by absent puberty and subsequent infertility due to gonadotropin-releasing hormone (GnRH) deficiency. IHH can be accompanied by normal or compromised olfaction (Kallmann syndrome