Ercan, Oya

Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor.

Farooqi, I. S., Wangensteen, T., Collins, S., Kimber, W., Matarese, G., Keogh, J. M., Lank, E., Bottomley, B., Lopez-Fernandez, J., Ferraz-Amaro, I., et al. (2007) · New England Journal of Medicine

Regulation of Appetite and ObesityHypothalamic control of reproductive hormones

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Homozygous Thyroid Hormone Receptor β-Gene Mutations in Resistance to Thyroid Hormone: Three New Cases and Review of the Literature

Ferrara, A. M., Onigata, K., Ercan, O., Woodhead, H., Weiss, R. E., & Refetoff, S. (2012) · The Journal of Clinical Endocrinology & Metabolism

Thyroid Disorders and TreatmentsGenomics and Rare Diseases

Cited by 110

Penile size in term newborn infants.

Akın, Y., Ercan, O., Telatar, B., & Tarhan, F. (2011) · The Turkish Journal of Pediatrics

Urological Disorders and TreatmentsGenital Health and Disease

Cited by 26

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