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Journal of Medical Genetics|January 1, 1991
Association of less common cystic fibrosis mutations with a mild phenotypeA Curtis, R Nelson, M Porteous, et al.Journal of Medical Genetics|July 7, 2000
The genetics of childhood cataractP J Francis, V Berry, S S Bhattacharya, et al.Dalton Transactions (Cambridge, England : 2003)|May 15, 2020
Role of size, alio-/multi-valency and non-stoichiometry in the synthesis of phase-pure high entropy oxide (Co,Cu,Mg,Na,Ni,Zn)ONandhini J Usharani, Rajat Shringi, Harshil Sanghavi, et al.Ophthalmic Research|January 1, 1997
Gene therapy for retinal degenerationM B Reichel, R R Ali, D M Hunt, et al.Investigative Ophthalmology & Visual Science|March 11, 2000
TGF-beta1, -beta2, and -beta3 in vitro: biphasic effects on Tenon's fibroblast contraction, proliferation, and migrationM F Cordeiro, S S Bhattacharya, G S Schultz, et al.Journal of Medical Genetics|December 1, 1994
Genetic heterogeneity in hereditary haemorrhagic telangiectasiaM E Porteous, A Curtis, O Williams, et al.Investigative Ophthalmology & Visual Science|December 1, 2001
Expression of Drosophila omb-related T-box genes in the developing human and mouse neural retinaJ C Sowden, J K Holt, M Meins, et al.Journal of Medical Genetics|September 11, 1998
Further refinement of the Usher 2A locus at 1q41D A Bessant, A M Payne, C Plant, et al.The Indian Journal of Medical Research|May 1, 1990
Susceptibility pattern of bacterial isolates to lomefloxacinM K Lalitha, A K Nisha, S S Bhattacharya, et al.Investigative Ophthalmology & Visual Science|August 1, 1997
Genomic organization of the human TIMP-1 gene. Investigation of a causative role in the pathogenesis of X-linked retinitis pigmentosa 2A J Hardcastle, D L Thiselton, M Nayudu, et al.Pageof 18