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Brain Research Bulletin|November 24, 2001
Trinucleotide repeat expansions: do they contribute to bipolar disorder?D Goossens, J Del-Favero, C Van BroeckhovenGene|March 30, 1999
YAC fragmentation with repetitive and single-copy sequences: detailed physical mapping of the presenilin 1 gene on chromosome 14J Del-Favero, D Goossens, D Van den Bossche, et al.Human Genetics|September 15, 2000
Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentationJ Del-Favero, D Goossens, P De Jonghe, et al.Human Genetics|December 22, 1999
Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degenerationA Michalík, J Del-Favero, C Mauger, et al.Molecular Psychiatry|June 21, 2007
Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish familiesT Venken, M Alaerts, D Souery, et al.Journal of the Neurological Sciences|September 29, 1999
Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian familyJ Martin, N Van Regemorter, J Del-Favero, et al.Brain Research. Molecular Brain Research|January 21, 2000
Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibodyC Mauger, J Del-Favero, C Ceuterick, et al.American Journal of Human Genetics|May 19, 2001
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancyL Claes, J Del-Favero, B Ceulemans, et al.Journal of Medical Genetics|April 14, 2005
A novel susceptibility locus at 2p24 for generalised epilepsy with febrile seizures plusD Audenaert, L Claes, K G Claeys, et al.Human Mutation|December 25, 2007
Progranulin locus deletion in frontotemporal dementiaI Gijselinck, J van der Zee, S Engelborghs, et al.Pageof 37