Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4003295 | American Journal of Ophthalmology | 2010 | 8 Pages |
Abstract
Patients with Duane syndrome and associated congenital malformations or developmental delay should be evaluated for the presence of underlying chromosomal duplications. The regions of chromosomes 2, 10, and 22 that we report may harbor genes involved in the pathogenesis of Duane syndrome.
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Authors
Sarah B. Smith, Elias I. Traboulsi,