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Journal of Medical Genetics|March 1, 2006
X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F geneR Jalkanen, M Mäntyjärvi, R Tobias, et al.The British Journal of Ophthalmology|June 21, 2005
Abnormal crossing of the optic fibres shown by evoked magnetic fields in patients with ocular albinism with a novel mutation in the OA1 geneL Lauronen, R Jalkanen, J Huttunen, et al.Journal of Medical Genetics|June 17, 2003
A new genetic locus for X linked progressive cone-rod dystrophyR Jalkanen, F Y Demirci, H Tyynismaa, et al.Pageof 1