Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kotan, Leman D."'
Autor:
Turan, Ihsan, Tastan, Mehmet, Boga, Duygu D., Gurbuz, Fatih, Kotan, Leman D., Tuli, Abdullah, Yüksel, Bilgin
Publikováno v:
In European Journal of Medical Genetics April 2020 63(4)
Autor:
Kotan, Leman D., Isik, Emregul, Turan, Ihsan, Mengen, Eda, Akkus, Gamze, Tastan, Mehmet, Gurbuz, Fatih, Yuksel, Bilgin, Topaloglu, A. Kemal
Idiopathic hypogonadotropic hypogonadism (IHH) can be divided into two major forms, normosmic IHH and Kallmann syndrome (KS). Genetic mutations are responsible for the majority of IHH. PLXNA1 has recently been implicated in the GnRH neuron migration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=r39c86a4b39b::0d65b5b6b96150f36591bc5161a0036c
https://aperta.ulakbim.gov.tr/record/68129
https://aperta.ulakbim.gov.tr/record/68129
Autor:
Kotan LD; Division of Pediatric Endocrinology, Cukurova University, Faculty of Medicine, Adana, Turkey., Isik E; Gaziantep Children's Hospital, Department of Pediatrics, Clinics of Pediatric Endocrinology, Gaziantep, Turkey., Turan I; Division of Pediatric Endocrinology, Cukurova University, Faculty of Medicine, Adana, Turkey., Mengen E; Department of Pediatrics, Division of Pediatric Endocrinology, Ankara Children's Hematology and Oncology Training Hospital, Ankara, Turkey., Akkus G; Division of Endocrinology, Cukurova University, Faculty of Medicine, Adana, Turkey., Tastan M; Division of Pediatric Endocrinology, Cukurova University, Faculty of Medicine, Adana, Turkey., Gurbuz F; Division of Pediatric Endocrinology, Cukurova University, Faculty of Medicine, Adana, Turkey., Yuksel B; Division of Pediatric Endocrinology, Cukurova University, Faculty of Medicine, Adana, Turkey., Topaloglu AK; Division of Pediatric Endocrinology, Cukurova University, Faculty of Medicine, Adana, Turkey.; Department of Pediatrics, Division of Pediatric Endocrinology, University of Mississippi Medical Center, Jackson, Mississippi.; Department of Neurobiology and Anatomical Sciences, University of Mississippi Medical Center, Jackson, Mississippi.
Publikováno v:
Clinical genetics [Clin Genet] 2019 Feb; Vol. 95 (2), pp. 320-324. Date of Electronic Publication: 2018 Dec 26.