| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4025964 | Ophthalmology | 2014 | 7 Pages |
Abstract
Our cases expand the ocular phenotype for duplication of 22q11 and serve to identify potential candidate genes for the development of CCDD, retinal vascular tortuosity, and glaucoma.
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Authors
Jose A. MD, Jenina MS, CGC, Michelle D. MD, Karthikeyan A. DNB, FRCS, George L. MD, Barry N. MD, Alex V. MD, MHSc,