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	1.	Retinal disease in mice lacking hypoxia-inducible transcription factor-2alpha. [electronic resource] by Ding, Kan Scortegagna, Marzia Seaman, Robyn Birch, David G Garcia, Joseph A Producer: 20050413 In: Investigative ophthalmology & visual science vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesis. [electronic resource] by Mues, Gabriele Tardivel, Aubry Willen, Laure Kapadia, Hitesh Seaman, Robyn Frazier-Bowers, Sylvia Schneider, Pascal D'Souza, Rena N Producer: 20100222 In: European journal of human genetics : EJHG vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families. [electronic resource] by Sullivan, Lori S Bowne, Sara J Birch, David G Hughbanks-Wheaton, Dianna Heckenlively, John R Lewis, Richard Alan Garcia, Charles A Ruiz, Richard S Blanton, Susan H Northrup, Hope Gire, Anisa I Seaman, Robyn Duzkale, Hatice Spellicy, Catherine J Zhu, Jingya Shankar, Suma P Daiger, Stephen P Producer: 20060807 In: Investigative ophthalmology & visual science vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)