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T Darras

Showing results (11-20 of 303) with videos related to

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American Journal of Human Genetics|August 1, 1988
Myopathy in complex glycerol kinase deficiency patients is due to 3' deletions of the dystrophin geneB T Darras, U Francke
Neurology|November 28, 2014
Congenital myopathies: Rebuilding the natural history, one gene at a timeEnrico Bertini, Basil T Darras
American Journal of Human Genetics|November 1, 1988
Normal human genomic restriction-fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNAB T Darras, U Francke
Nature|October 8, 1987
A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected maleB T Darras, U Francke
Neurology|September 18, 2013
Predicting hearing loss in facioscapulohumeral muscular dystrophyBasil T Darras, Rabi Tawil
Revue De Pneumologie Clinique|January 1, 1990
[Recurrent plate atelectasis. Apropos of a case]P Gilbert, J Jaucot, T Darras
Neurological Research|March 1, 1992
Loss of heterozygosity on the short arm of chromosome 17 in human astrocytomasJ K Wu, B T Darras
Pediatric Neurology|August 1, 2006
Catecholamine toxicity in aromatic L-amino acid decarboxylase deficiencyIrina A Anselm, Basil T Darras
Neurology|January 4, 2013
Making sense of genetic heterogeneity: Emergence of pathways in developmental brain disordersAlex R Paciorkowski, Basil T Darras
Journal of Physics. Conference Series|July 30, 2013
Electrical impedance myography for the assessment of children with muscular dystrophy: a preliminary studyS B Rutkove, B T Darras
Pageof 31

Showing results (11-20 of 303) with videos related to

Sort By:
Pageof 31
American Journal of Human Genetics|August 1, 1988
Myopathy in complex glycerol kinase deficiency patients is due to 3' deletions of the dystrophin geneB T Darras, U Francke
Neurology|November 28, 2014
Congenital myopathies: Rebuilding the natural history, one gene at a timeEnrico Bertini, Basil T Darras
American Journal of Human Genetics|November 1, 1988
Normal human genomic restriction-fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNAB T Darras, U Francke
Nature|October 8, 1987
A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected maleB T Darras, U Francke
Neurology|September 18, 2013
Predicting hearing loss in facioscapulohumeral muscular dystrophyBasil T Darras, Rabi Tawil
Revue De Pneumologie Clinique|January 1, 1990
[Recurrent plate atelectasis. Apropos of a case]P Gilbert, J Jaucot, T Darras
Neurological Research|March 1, 1992
Loss of heterozygosity on the short arm of chromosome 17 in human astrocytomasJ K Wu, B T Darras
Pediatric Neurology|August 1, 2006
Catecholamine toxicity in aromatic L-amino acid decarboxylase deficiencyIrina A Anselm, Basil T Darras
Neurology|January 4, 2013
Making sense of genetic heterogeneity: Emergence of pathways in developmental brain disordersAlex R Paciorkowski, Basil T Darras
Journal of Physics. Conference Series|July 30, 2013
Electrical impedance myography for the assessment of children with muscular dystrophy: a preliminary studyS B Rutkove, B T Darras
Pageof 31