Bereket, Abdullah

Rare causes of primary adrenal insufficiency: genetic and clinical characterization of a large nationwide cohort

Guran, T., Buonocore, F., Saka, N., Ozbek, M. N., Aycan, Z., Bereket, A., Bas, F., Darcan, S., Bideci, A., Guven, A., et al. (2016) · The Journal of Clinical Endocrinology & Metabolism

Adrenal Hormones and DisordersSexual Differentiation and Disorders

Cited by 207

Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and “Apparent” Thyroid Dysgenesis

Kühnen, P., Turan, S., Fröhler, S., Güran, T., Abali, S., Biebermann, H., Bereket, A., Grüters, A., Chen, W., & Krude, H. (2014) · The Journal of Clinical Endocrinology & Metabolism

Thyroid Disorders and TreatmentsHead and Neck Anomalies

Cited by 63

Adrenal steroids reference ranges in infancy determined by LC-MS/MS

Enver, E. O., Vatansever, P., Guran, O., Bilgin, L., Boran, P., Turan, S., Haklar, G., Bereket, A., & Guran, T. (2022) · Pediatric Research

Adrenal Hormones and DisordersMetabolism and Genetic Disorders

Cited by 12

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

Sari, E., Bereket, A., Yeşilkaya, E., Baş, F., Bundak, R., Aydın, B. K., Darcan, Ş., Dündar, B., Büyükinan, M., Kara, C., et al. (2016) · American Journal of Medical Genetics Part A

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesSexual Differentiation and Disorders

Cited by 11