Your search returned 28 results.

Results
	21.	Low frequency of myocilin mutations in Indian primary open-angle glaucoma patients. [electronic resource] by Sripriya, S Uthra, S Sangeetha, R George, R J Hemamalini, A Paul, P G Amali, J Vijaya, L Kumaramanickavel, G Producer: 20040617 In: Clinical genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Inducible nitric oxide synthase gene and diabetic retinopathy in Asian Indian patients. [electronic resource] by Kumaramanickavel, G Sripriya, S Vellanki, R N Upadyay, N K Badrinath, S S Rajendran, V Sukumar, B Ramprasad, V L Sharma, T Producer: 20020924 In: Clinical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3. [electronic resource] by Finckh, U Xu, S Kumaramanickavel, G Schürmann, M Mukkadan, J K Fernandez, S T John, S Weber, J L Denton, M J Gal, A Producer: 19980608 In: Genomics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	OPTN gene: profile of patients with glaucoma from India. [electronic resource] by Sripriya, S Nirmaladevi, J George, R Hemamalini, A Baskaran, M Prema, R Ve Ramesh, S Karthiyayini, T Amali, J Job, S Vijaya, L Kumaramanickavel, G Producer: 20060921 In: Molecular vision vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	25.	Tumor necrosis factor allelic polymorphism with diabetic retinopathy in India. [electronic resource] by Kumaramanickavel, G Sripriya, S Vellanki, R N Upadyay, N K Badrinath, S S Arokiasamy, T Sukumar, B Vidhya, A Joseph, B Sharma, T Gopal, L Producer: 20020116 In: Diabetes research and clinical practice vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy. [electronic resource] by Gu, S M Thompson, D A Srikumari, C R Lorenz, B Finckh, U Nicoletti, A Murthy, K R Rathmann, M Kumaramanickavel, G Denton, M J Gal, A Producer: 19971114 In: Nature genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration. [electronic resource] by Maw, M A Corbeil, D Koch, J Hellwig, A Wilson-Wheeler, J C Bridges, R J Kumaramanickavel, G John, S Nancarrow, D Röper, K Weigmann, A Huttner, W B Denton, M J Producer: 20000229 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin gene. [electronic resource] by Klintworth, G K Sommer, J R Obrian, G Han, L Ahmed, M N Qumsiyeh, M B Lin, P Y Basti, S Reddy, M K Kanai, A Hotta, Y Sugar, J Kumaramanickavel, G Munier, F Schorderet, D F El Matri, L Iwata, F Kaiser-Kupfer, M Nagata, M Nakayasu, K Hejtmancik, J F Teng, C T Producer: 19990114 In: Molecular vision vol. 4 Availability: No items available. Save to lists Add to cart (remove)