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Human Mutation|January 1, 1995
Déjérine-Sottas neuropathy is associated with a de novo PMP22 mutationL J Valentijn, R A Ouvrier, N H van den Bosch, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Muscle cell cultures in Menkes' disease: copper accumulation in myotubesG J van den Berg, J J Kroon, F A Wijburg, et al.
American Journal of Human Genetics|April 1, 1997
Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21A J van der Kooi, M van Meegen, T M Ledderhof, et al.
American Journal of Human Genetics|May 9, 2003
Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathyNeil Howell, Roelof-Jan Oostra, Piet A Bolhuis, et al.
Neurology|March 1, 1996
Genetic localization of Bethlem myopathyG J Jobsis, P A Bolhuis, J M Boers, et al.
Biochimica Et Biophysica Acta|February 21, 1992
Isoforms of cytochrome c oxidase in tissues and cell lines of the mouseC Van den Bogert, H L Dekker, J C Cornelissen, et al.
Applied and Environmental Microbiology|July 2, 1999
Evaluation of bottlenecks in the late stages of protein secretion in Bacillus subtilisA Bolhuis, H Tjalsma, H E Smith, et al.
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