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Strabismus, CCDD and Other Anomalies

Recent Progress in Understanding Congenital Cranial Dysinnervation Disorders

D. Oystreck, E. Engle, T. Bosley. (2011). Journal of Neuro-Ophthalmology. Cited 80 times. https://doi.org/10.1097/WNO.0b013e31820d0756

HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice.

B. Webb, S. Shaaban, H. Gaspar, et al. (2012). American journal of human genetics. Cited 77 times. https://doi.org/10.1016/j.ajhg.2012.05.018