For citations:
Kalinchenko N.Yu., Kolodkina A.A., Raygorodskaya N.Y., Tiulpakov A.N. Clinical and molecular characteristics of patients with 46,XY DSD due to NR5A1 gene mutations. Problems of Endocrinology. 2020;66(3):62-69. https://doi.org/10.14341/probl12445
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