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	1.	A novel mutation in ACTG1 causing Baraitser-Winter syndrome with extremely variable expressivity in three generations. [electronic resource] by Kemerley, Andrew Sloan, Christina Pfeifer, Wanda Smith, Richard Drack, Arlene Producer: 20171113 In: Ophthalmic genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Vitritis in pediatric genetic retinal disorders. [electronic resource] by Stunkel, Maria Bhattarai, Sajag Kemerley, Andrew Stone, Edwin M Wang, Kai Mullins, Robert F Drack, Arlene V Producer: 20150312 In: Ophthalmology vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Correlation between electroretinography, foveal anatomy and visual acuity in albinism. [electronic resource] by Hu, Zhaohui Wang, Kai Bertsch, Morgan Dunn, Taylor Kehoe, Taylor Kemerley, Andrew D Helms, Megan Bhattarai, Sajag Pfeifer, Wanda Scheetz, Todd E Drack, Arlene V Producer: 20190830 In: Documenta ophthalmologica. Advances in ophthalmology vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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