Cite
HARVARD Citation
Reis, L. et al. (n.d.). A Case of 22q11.2 Deletion Syndrome with Peters Anomaly, Congenital Glaucoma, and Heterozygous Mutation in CYP1B1. Ophthalmic genetics. pp. 92-94. [Online].
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Reis, L. et al. (n.d.). A Case of 22q11.2 Deletion Syndrome with Peters Anomaly, Congenital Glaucoma, and Heterozygous Mutation in CYP1B1. Ophthalmic genetics. pp. 92-94. [Online].