Güven Toksoy

Cleidocranial dysplasia: Clinical, endocrinologic and molecular findings in 15 patients from 11 families

Firdevs Dinçsoy Bir, Nuriye Dinçkan, Yeliz Güven et al. · European Journal of Medical Genetics · 2016 · 38 citations

Medicine, Craniofacial Biology, Endocrinology +13

A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations

Aslı Derya Kardelen, Güven Toksoy, Firdevs Baş et al. · Journal of Clinical Research in Pediatric Endocrinology · 2018 · 37 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene

Firdevs Baş, Güven Toksoy, Berrin Ergun-Longmire et al. · The Journal of Steroid Biochemistry and Molecular Biology · 2018 · 32 citations

Life Sciences, Endocrinology, Genetics +17

Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases

Birsen Karaman, Hülya Kayserili, Asadollah Ghanbari et al. · Molecular Cytogenetics · 2018 · 30 citations · Full text

Life Sciences, Molecular Genetics, Cytogenetics +14

Prevalence of X-aneuploidies, X-structural abnormalities and 46,XY sex reversal in Turkish women with primary amenorrhea or premature ovarian insufficiency

Bilgen Bilge Geçkinli, Güven Toksoy, Ceyhan Sayar et al. · European Journal of Obstetrics & Gynecology and Reproductive Biology · 2014 · 29 citations

Medicine, Endocrinology, Gynecology +13