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Ophthalmic Genetics|March 1, 1994
The electrooculogram in heterozygote carriers of Usher syndrome, retinitis pigmentosa, neuronal ceroid lipofuscinosis, senior syndrome and choroideremiaA Pinckers, A van Aarem, H BrinkOphthalmic Genetics|September 1, 1994
Radial asymmetry in the topography of retinoblastoma. Clues to the cell of originF L Munier, A Balmer, G van Melle, et al.Ophthalmic Genetics|September 1, 1994
Recurrence of unilateral retinoblastoma following radiation therapyD H Abramson, C A Servodidio, A R De Lillo, et al.Ophthalmic Genetics|September 1, 1994
Balanced translocation (t 2q; 10p) and ocular anomalies. A possible HOX gene defectP Nucci, M P Manitto, A Faiella, et al.Ophthalmic Genetics|September 1, 1994
Iris melanoma in a ten-year-old boy with familial atypical mole-melanoma (FAM-M) syndromeA D Singh, J A Shields, R C Eagle, et al.Ophthalmic Genetics|December 15, 2005
Coats-type retinal telangiectasia in case of Kabuki make-up syndrome (Niikawa-Kuroki syndrome)M Anandan, Neroli J Porter, Andrea H Nemeth, et al.Ophthalmic Genetics|December 15, 2005
The relative contribution of the X chromosome to ocular phenotypesA W Hewitt, K P BurdonOphthalmic Genetics|February 10, 2010
Protein kinase C beta (PRKCB1) and pigment epithelium derived factor (PEDF) gene polymorphisms and diabetic retinopathy in a south Indian cohortSatagopan Uthra, Rajiv Raman, Bickol N Mukesh, et al.Pageof 185