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	1.	Gene symbol: CYP1B1. Disease: Primary congenital glaucoma. Accession #Hd0515. [electronic resource] by Nirmaladevi, J Karthiyayini, T Kumaramanickavel, G Producer: 20070309 In: Human genetics vol. 118 Availability: No items available. Save to lists Add to cart (remove)
	2.	Gene symbol: CYP1B1. Disease: Primary congenital glaucoma. Accession #Hm0544. [electronic resource] by Nirmaladevi, J Karthiyayini, T Kumaramanickavel, G Producer: 20070309 In: Human genetics vol. 118 Availability: No items available. Save to lists Add to cart (remove)
	3.	Retinitis pigmentosa in India: a genetic and segregation analysis. [electronic resource] by Kar, B John, S Kumaramanickavel, G Producer: 19950815 In: Clinical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	No evidence for a genetic blueprint: The case of the "complex" mammalian photoreceptor. [electronic resource] by Kumaramanickavel, G Denton, M J Legge, M Producer: 20161213 In: Indian journal of ophthalmology vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Gene symbol: PRPF31. [electronic resource] by Mamatha, G Venkataramana, A Srilekha, S Kumaramanickavel, G Producer: 20070502 In: Human genetics vol. 120 Availability: No items available. Save to lists Add to cart (remove)
	6.	Genetic analysis of adult-onset cataract in a city-based ophthalmic hospital. [electronic resource] by Vijaya, R Gupta, R Panda, G Ravishankar, K Kumaramanickavel, G Producer: 19980430 In: Clinical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Consanguinity and ocular genetic diseases in South India: analysis of a five-year study. [electronic resource] by Kumaramanickavel, G Joseph, B Vidhya, A Arokiasamy, T Shridhara Shetty, N Producer: 20040302 In: Community genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Retinitis pigmentosa patients with sickle cell disease and dextrocardia and situs inversus syndrome. [electronic resource] by Madhavan, C Bhende, P Gopal, L Vasanthi, S B Kumaramanickavel, G Producer: 20050602 In: Indian journal of ophthalmology vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	9.	Two Indian siblings with Oguchi disease are homozygous for an arrestin mutation encoding premature termination. [electronic resource] by Maw, M Kumaramanickavel, G Kar, B John, S Bridges, R Denton, M Producer: 19990630 In: Human mutation vol. Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian family. [electronic resource] by Gu, S Kumaramanickavel, G Srikumari, C R Denton, M J Gal, A Producer: 19991027 In: Journal of medical genetics vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	11.	Prevalence of Childhood Blindness and Ocular Morbidity in a Rural Pediatric Population in Southern India: The Pavagada Pediatric Eye Disease Study-1. [electronic resource] by Kemmanu, Vasudha Hegde, Kaushik Giliyar, Subramanya K Shetty, Bhujanga K Kumaramanickavel, G McCarty, Catherine A Producer: 20170718 In: Ophthalmic epidemiology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Genetic profile of 81 retinoblastoma patients from a referral hospital in southern India. [electronic resource] by Harini, R Ata-ur-Rasheed, M Shanmugam, M P Amali, J Das, D Kumaramanickavel, G Producer: 20050607 In: Indian journal of ophthalmology vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	13.	The pavagada pediatric eye disease study: objectives, methodology and participant characteristics. [electronic resource] by Kemmanu, Vasudha Hegde, Kaushik Devagirkar, Smitha Pujar, Chandrakant Shetty, Bhujang K Kumaramanickavel, G McCarty, Catherine A Producer: 20131213 In: Ophthalmic epidemiology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Parental inability to detect eye diseases in children: barriers to access of childhood eye-care services in south India. [electronic resource] by Kemmanu, V Giliyar, S K Shetty, B K Singh, A K Kumaramanickavel, G McCarty, C A Producer: 20180905 In: Eye (London, England) vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22. [electronic resource] by Dollfus, H Kumaramanickavel, G Biswas, P Stoetzel, C Quillet, R Denton, M Maw, M Perrin-Schmitt, F Producer: 20011205 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Oguchi disease: suggestion of linkage to markers on chromosome 2q. [electronic resource] by Maw, M A John, S Jablonka, S Müller, B Kumaramanickavel, G Oehlmann, R Denton, M J Gal, A Producer: 19950823 In: Journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Missense rhodopsin mutation in a family with recessive RP. [electronic resource] by Kumaramanickavel, G Maw, M Denton, M J John, S Srikumari, C R Orth, U Oehlmann, R Gal, A Producer: 19950106 In: Nature genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Linkage of blepharophimosis syndrome in a large Indian pedigree to chromosome 7p. [electronic resource] by Maw, M Kar, B Biswas, J Biswas, P Nancarrow, D Bridges, R Kumaramanickavel, G Denton, M Badrinath, S S Producer: 19970314 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Mutation spectrum in BBS genes guided by homozygosity mapping in an Indian cohort. [electronic resource] by Sathya Priya, C Sen, P Umashankar, V Gupta, N Kabra, M Kumaramanickavel, G Stoetzel, C Dollfus, H Sripriya, S Producer: 20150916 In: Clinical genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Prevalence and causes of blindness in the rural population of the Chennai Glaucoma Study. [electronic resource] by Vijaya, L George, R Arvind, H Baskaran, M Raju, P Ramesh, S V Paul, P G Kumaramanickavel, G McCarty, C Producer: 20060413 In: The British journal of ophthalmology vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 28 results.