Article Versions Notes

de Oliveira-Sobrinho RP, Appenzeller S, Holanda IP, Heleno JL, Jorente J, on behalf of the Rare Genomes Project Consortium, Vieira TP, Steiner CE. Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis. Genes. 2024; 15(4):513. https://doi.org/10.3390/genes15040513

de Oliveira-Sobrinho, Ruy Pires, Simone Appenzeller, Ianne Pessoa Holanda, Júlia Lôndero Heleno, Josep Jorente, on behalf of the Rare Genomes Project Consortium, Társis Paiva Vieira, and Carlos Eduardo Steiner. 2024. "Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis" Genes 15, no. 4: 513. https://doi.org/10.3390/genes15040513

de Oliveira-Sobrinho, R. P., Appenzeller, S., Holanda, I. P., Heleno, J. L., Jorente, J., on behalf of the Rare Genomes Project Consortium, Vieira, T. P., & Steiner, C. E. (2024). Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis. Genes, 15(4), 513. https://doi.org/10.3390/genes15040513