E. D. Çakır

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

F. Baş, F. Darendeliler, F. Demirel, 2016, American journal of medical genetics. Part A.

Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

S. Poyrazoglu, F. Baş, F. Darendeliler, 2015, Journal of clinical research in pediatric endocrinology.

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

F. Baş, F. Darendeliler, F. Demirel, 2015, Journal of clinical research in pediatric endocrinology.

Loss-of-Function Mutations in SEMA3F and gePLXNA3 Encoding Semaphorin-3F and its Receptor Plexin-A3 Respectively Cause Idiopathic Hypogonadotropic Hypogonadism

F. Darendeliler, A. Topaloğlu, L. D. Kotan, 2022 .

Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

F. Darendeliler, A. Topaloğlu, L. D. Kotan, 2021, Genetics in Medicine.

Retrospective evaluation of pubertal development and linear growth of girls with Turner Syndrome treated with oral and transdermal estrogen

E. Eren, H. Sağlam, Ö. Tarım, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal-recessive hypophosphataemic rickets type 2.

A. Çayır, Elvan Bayramoğlu, E. D. Çakır, 2024, Clinical endocrinology.