Article ID Journal Published Year Pages File Type
4003295 American Journal of Ophthalmology 2010 8 Pages PDF
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.
Related Topics
Health Sciences Medicine and Dentistry Ophthalmology
Authors
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