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	41.	Optic atrophy in Marinesco-Sjögren syndrome: an additional ocular feature. Report of three cases in two families. [electronic resource] by Dotti, M T Bardelli, A M De Stefano, N Federico, A Malandrini, A Vanni, M Guazzi, G C Producer: 19930907 In: Ophthalmic paediatrics and genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation. [electronic resource] by Malandrini, A Mari, F Palmeri, S Gambelli, S Berti, G Bruttini, M Bardelli, A M Williamson, K van Heyningen, V Renieri, A Producer: 20011011 In: Clinical genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Coats disease: smaller volume of the affected globe. [electronic resource] by Galluzzi, P Venturi, C Cerase, A Vallone, I M Bracco, S Bardelli, A M Hadjistilianou, T Gennari, P Monti, L Filosomi, G Producer: 20011101 In: Radiology vol. 221 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	Pseudoxanthoma elasticum: Point mutations in the ABCC6 gene and a large deletion including also ABCC1 and MYH11. [electronic resource] by Meloni, I Rubegni, P De Aloe, G Bruttini, M Pianigiani, E Cusano, R Seri, M Mondillo, S Federico, A Bardelli, A M Andreassi, L Fimiani, M Renieri, A Producer: 20011212 In: Human mutation vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)