Showing results (151-160 of 161) with videos related to
Sort By:
Pageof 17
American Journal of Human Genetics|January 1, 1996
The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15qL K Casaubon, M Melanson, I Lopes-Cendes, et al.Neurology|February 1, 1990
Tight linkage of creatine kinase (CKMM) to myotonic dystrophy on chromosome 19L H Yamaoka, M A Pericak-Vance, M C Speer, et al.Social Science & Medicine (1982)|March 1, 1996
Alzheimer's disease: preliminary study of spatial distribution at birth placeH Jean, J F Emard, J P Thouez, et al.Brain : a Journal of Neurology|May 5, 2006
A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34I Thiffault, M F Rioux, M Tetreault, et al.American Journal of Human Genetics|March 3, 1999
Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11A Richter, J D Rioux, J P Bouchard, et al.Nature Genetics|February 2, 2000
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORFJ C Engert, P Bérubé, J Mercier, et al.Frontiers in Tuberculosis|June 3, 2026
Dose optimization of inhaled tigecycline in humans to overcome inherent adverse events and maximize bacterial clearance using a physiologically-based pharmacokinetic modeling approachHyunseo Park, Amarinder Singh, Ashish Srivastava, et al.Nature Communications|February 9, 2019
Folliculin regulates mTORC1/2 and WNT pathways in early human pluripotencyJ Mathieu, D Detraux, D Kuppers, et al.Nature Genetics|February 14, 1998
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyB Brais, J P Bouchard, Y G Xie, et al.The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 20, 2012
Diversity of ARSACS mutations in French-CanadiansI Thiffault, M J Dicaire, M Tetreault, et al.Pageof 17