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