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The British Journal of Ophthalmology|August 1, 1993
Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsinE Apfelstedt-Sylla, M Kunisch, M Horn, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1988
[Concordance of Kearns-Sayre syndrome and Klinefelter syndrome]A S Everding, G Kurlemann, H Gerding, et al.Pageof 8