Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author exact 801000441207 cql: author exact 801000365425 Add to list Journal Article A1 A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome. S SENECA, H VERHELST, L DE MEIRLEIR, Françoise Meire (UGent) , C GROOTE, W LISSENS and Rudy Van Coster (UGent) (2001) ARCHIVES OF NEUROLOGY. 58(7). p.1113-1118 Add to list Journal Article A1 Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation: A new example of the Chitty syndrome. SG VANDAELE, Rudy Van Coster (UGent) , Françoise Meire (UGent) , AM SMETS and Juliaan Leroy (UGent) (1996) AMERICAN JOURNAL OF MEDICAL GENETICS. 65(3). p.205-208 Add to list Journal Article A1 Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutations. Françoise Meire (UGent) , Rudy Van Coster (UGent) , P COCHAUX, B OBERMAIERKUSSER, C CANDAELE and JJ MARTIN (1995) OPHTHALMIC GENETICS. 16(3). p.119-126