M, D. V., A, M., D, E., K, G., JA, T., A, V., . . . W, Z. (2025). Urofacial (Ochoa) syndrome with a founder pathogenic variant in the HPSE2 gene: A case report and mutation origin. Journal of applied genetics, 66(3), 637. https://doi.org/10.1007/s13353-024-00896-7
Chicago Style (17th ed.) CitationM, Del Valle-Peréz, et al. "Urofacial (Ochoa) Syndrome with a Founder Pathogenic Variant in the HPSE2 Gene: A Case Report and Mutation Origin." Journal of Applied Genetics 66, no. 3 (2025): 637. https://doi.org/10.1007/s13353-024-00896-7.
MLA (9th ed.) CitationM, Del Valle-Peréz, et al. "Urofacial (Ochoa) Syndrome with a Founder Pathogenic Variant in the HPSE2 Gene: A Case Report and Mutation Origin." Journal of Applied Genetics, vol. 66, no. 3, 2025, p. 637, https://doi.org/10.1007/s13353-024-00896-7.