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	1.	The cost of genetic testing for ocular disease: who pays? [electronic resource] by Capasso, Jenina E Producer: 20141014 In: Current opinion in ophthalmology vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Ocular manifestations of Emanuel syndrome. [electronic resource] by Saffren, Brooke D Capasso, Jenina E Zanolli, Mario Levin, Alex V Producer: 20190911 In: American journal of medical genetics. Part A vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Lyonization in ophthalmology. [electronic resource] by Wuthisiri, Wadakarn Lingao, Michelle D Capasso, Jenina E Levin, Alex V Producer: 20131025 In: Current opinion in ophthalmology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Intraretinal cystoid spaces in a patient with retinitis pigmentosa due to mutation in the MAK gene. [electronic resource] by Lai, Yu-Hung Capasso, Jenina E Kaiser, Richard Levin, Alex V Producer: 20171106 In: Ophthalmic genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Early onset ectopia lentis due to a FBN1 mutation with non-penetrance. [electronic resource] by Zhang, Li Lai, Yu-Hung Capasso, Jenina E Han, Stella Levin, Alex V Producer: 20160217 In: American journal of medical genetics. Part A vol. 167 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and Son. [electronic resource] by Arcot Sadagopan, Karthikeyan Battista, Robert Keep, Rosanne B Capasso, Jenina E Levin, Alex V Producer: 20160223 In: Ophthalmic genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Ocular manifestations of PACS1 mutation. [electronic resource] by Pefkianaki, Maria Schneider, Adele Capasso, Jenina E Wasserman, Barry N Bardakjian, Tanya Levin, Alex V Producer: 20190909 In: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Anirdia-like phenotype caused by 6p25 dosage aberrations. [electronic resource] by Sadagopan, Karthikeyan Arcot Liu, Grace T Capasso, Jenina E Wuthisiri, Wadakarn Keep, Rosanne B Levin, Alex V Producer: 20160429 In: American journal of medical genetics. Part A vol. 167A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Organophosphate retinopathy. [electronic resource] by Pham, Hang Lingao, Michelle D Ganesh, Anuradha Capasso, Jenina E Keep, Rosanne Sadagopan, Karthikeyan A Levin, Alex V Producer: 20160325 In: Oman journal of ophthalmology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Peters anomaly in cri-du-chat syndrome. [electronic resource] by Hope, William C Cordovez, Jose A Capasso, Jenina E Hammersmith, Kristin M Eagle, Ralph C Lall-Trail, Joel Levin, Alex V Producer: 20160120 In: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Retinal Dystrophy with Intraretinal Cystoid Spaces Associated with Mutations in the Crumbs Homologue (CRB1) Gene. [electronic resource] by Cordovez, Jose A Traboulsi, Elias I Capasso, Jenina E Sadagopan, Karthikeyan Arcot Ganesh, Anuradha Rychwalski, Paul J Neely, Kimberly A Brodie, Scott E Levin, Alex V Producer: 20160401 In: Ophthalmic genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Spectrum of PEX1 and PEX6 variants in Heimler syndrome. [electronic resource] by Smith, Claire E L Poulter, James A Levin, Alex V Capasso, Jenina E Price, Susan Ben-Yosef, Tamar Sharony, Reuven Newman, William G Shore, Roger C Brookes, Steven J Mighell, Alan J Inglehearn, Chris F Producer: 20170707 In: European journal of human genetics : EJHG vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach. [electronic resource] by Petersen-Jones, Simon M Occelli, Laurence M Winkler, Paige A Lee, Winston Sparrow, Janet R Tsukikawa, Mai Boye, Sanford L Chiodo, Vince Capasso, Jenina E Becirovic, Elvir Schön, Christian Seeliger, Mathias W Levin, Alex V Michalakis, Stylianos Hauswirth, William W Tsang, Stephen H Producer: 20190507 In: The Journal of clinical investigation vol. 128 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)