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Journal of Clinical Research in Pediatric Endocrinology|April 19, 2022
Comparative Analyses of Turkish Variome and Widely Used Genomic Variation Databases for the Evaluation of Rare Sequence Variants in Turkish Individuals: Idiopathic Hypogonadotropic Hypogonadism as a Disease ModelLeman Damla KotanEndocrine Development|December 19, 2015
Genetics of Hypogonadotropic HypogonadismA Kemal Topaloglu, L Damla KotanJournal of Clinical Research in Pediatric Endocrinology|September 17, 2025
Genetics of Idiopathic Hypogonadotropic HypogonadismA Kemal Topaloğlu, Leman Damla KotanCurrent Opinion in Obstetrics & Gynecology|June 15, 2010
Molecular causes of hypogonadotropic hypogonadismAli Kemal Topaloglu, Leman Damla KotanJournal of the College of Physicians and Surgeons--Pakistan : JCPSP|April 26, 2018
A Novel Frameshift Mutation in ESCO2 Gene in Roberts SyndromeEda Mengen, Leman Damla Kotan, Seyit Ahmet Ucakturk, et al.Journal of Clinical Research in Pediatric Endocrinology|January 18, 2020
Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone DeficiencyFatma Derya Bulut, Semine Özdemir Dilek, Damla Kotan, et al.American Journal of Medical Genetics. Part A|December 1, 2022
A novel homozygous nonsense NDNF variant in Kallmann syndromeLeman Damla Kotan, Melek Yildiz, Ihsan Turan, et al.Clinical Endocrinology|March 28, 2018
Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistanceIhsan Turan, Leman Damla Kotan, Mehmet Tastan, et al.Endocrine|May 17, 2025
An evaluation of cases of disorders of sex development related to SRD5A2Can Celiloglu, Ihsan Turan, Leman Damla Kotan, et al.Hormone Research in Paediatrics|October 25, 2021
DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic HypogonadismIhsan Turan, Korcan Demir, Eda Mengen, et al.Pageof 4