Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.


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Akcan N., Uyguner Z. O., Bas F., Altunoglu U., Toksoy G., Karaman B., ...Daha Fazla

Journal of clinical research in pediatric endocrinology, cilt.14, sa.2, ss.153-171, 2022 (SCI-Expanded) identifier identifier identifier