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Serpen JY, Presley W, Beil A, Armenti ST, Johnson K, Mian SI, Innis JW, Prasov L. A Novel 13q12 Microdeletion Associated with Familial Syndromic Corneal Opacification. Genes. 2023; 14(5):1034. https://doi.org/10.3390/genes14051034

Serpen, Jasmine Y., William Presley, Adelyn Beil, Stephen T. Armenti, Kayla Johnson, Shahzad I. Mian, Jeffrey W. Innis, and Lev Prasov. 2023. "A Novel 13q12 Microdeletion Associated with Familial Syndromic Corneal Opacification" Genes 14, no. 5: 1034. https://doi.org/10.3390/genes14051034

Serpen, J. Y., Presley, W., Beil, A., Armenti, S. T., Johnson, K., Mian, S. I., Innis, J. W., & Prasov, L. (2023). A Novel 13q12 Microdeletion Associated with Familial Syndromic Corneal Opacification. Genes, 14(5), 1034. https://doi.org/10.3390/genes14051034