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de Sousa Azulay RS, Facundo AN, Sousa SSe, Nascimento GC, Magalhães M, de Oliveira Neto CP, de Abreu JDMF, Lago DCF, da Silva Pereira Damianse S, de Carvalho VC, et al. Unique Case Report: A Rare Association of 21-Hydroxylase Deficiency with Triple X Karyotype. Genes. 2025; 16(3):354. https://doi.org/10.3390/genes16030354

de Sousa Azulay, Rossana Santiago, Alexandre Nogueira Facundo, Sarah Sousa e Sousa, Gilvan Cortes Nascimento, Marcelo Magalhães, Clariano Pires de Oliveira Neto, Joana D’arc Matos França de Abreu, Débora Cristina Ferreira Lago, Sabrina da Silva Pereira Damianse, Viviane Chaves de Carvalho, and et al. 2025. "Unique Case Report: A Rare Association of 21-Hydroxylase Deficiency with Triple X Karyotype" Genes 16, no. 3: 354. https://doi.org/10.3390/genes16030354

de Sousa Azulay, R. S., Facundo, A. N., Sousa, S. S. e., Nascimento, G. C., Magalhães, M., de Oliveira Neto, C. P., de Abreu, J. D. M. F., Lago, D. C. F., da Silva Pereira Damianse, S., de Carvalho, V. C., Nascimento, C. A., Rodrigues, V. P., Coeli-Lacchini, F. B., de Castro, M., & dos Santos Faria, M. (2025). Unique Case Report: A Rare Association of 21-Hydroxylase Deficiency with Triple X Karyotype. Genes, 16(3), 354. https://doi.org/10.3390/genes16030354