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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|August 10, 2004
Respiratory insufficiency as a presenting symptom of LGMD2D in adulthoodM C Walter, G Dekomien, B Schlotter-Weigel, et al.
Genes and Immunity|April 9, 2005
Association of multiple sclerosis with ILT6 deficiencyS Koch, R Goedde, V Nigmatova, et al.
Annals of the Rheumatic Diseases|October 31, 2007
The Wegener's granulomatosis quantitative trait locus on chromosome 6p21.3 as characterised by tagSNP genotypingM Heckmann, J U Holle, L Arning, et al.
Genes, Chromosomes & Cancer|February 1, 1993
Detection of somatic changes in human renal cell carcinomas with oligonucleotide probes specific for simple repeat motifsS Bock, J T Epplen, H Noll-Puchta, et al.
American Journal of Medical Genetics|July 14, 1999
Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsyT Sander, C Peters, G Kämmer, et al.
Brain Pathology (Zurich, Switzerland)|November 6, 1998
An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patientsT Schmidt, G B Landwehrmeyer, I Schmitt, et al.
Neuroreport|August 16, 2000
Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's diseaseR Krüger, A M Menezes-Saecker, L Schöls, et al.
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