EE, B., KJ, M., KE, N., TA, D., SL, C., JJ, W., . . . AF, O. (2024). Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study. Birth defects research, 116(7), e2384. https://doi.org/10.1002/bdr2.2384
Chicago Style (17th ed.) CitationEE, Blue, et al. "Exome Sequencing Identifies Novel Genes Underlying Primary Congenital Glaucoma in the National Birth Defects Prevention Study." Birth Defects Research 116, no. 7 (2024): e2384. https://doi.org/10.1002/bdr2.2384.
MLA (9th ed.) CitationEE, Blue, et al. "Exome Sequencing Identifies Novel Genes Underlying Primary Congenital Glaucoma in the National Birth Defects Prevention Study." Birth Defects Research, vol. 116, no. 7, 2024, p. e2384, https://doi.org/10.1002/bdr2.2384.