Akcan, N. Et Al. 2022. Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.. Journal of clinical research in pediatric endocrinology , vol.14, no.2 , 153-171.

Akcan, N., Uyguner, Z. O., Bas, F., Altunoglu, U., Toksoy, G., Karaman, B., ... Avci, S.(2022). Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.. Journal of clinical research in pediatric endocrinology , vol.14, no.2, 153-171.

Akcan, Nese Et Al. "Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.," Journal of clinical research in pediatric endocrinology , vol.14, no.2, 153-171, 2022

Akcan, Nese Et Al. "Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.." Journal of clinical research in pediatric endocrinology , vol.14, no.2, pp.153-171, 2022

Akcan, N. Et Al. (2022) . "Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.." Journal of clinical research in pediatric endocrinology , vol.14, no.2, pp.153-171.

@article{article, author={Nese Akcan Et Al. }, title={Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.}, journal={Journal of clinical research in pediatric endocrinology}, year=2022, pages={153-171} }