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Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|December 1, 1995
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2A Helbling-Leclerc, H Topaloglu, F M Tomé, et al.Neuromuscular Disorders : NMD|March 1, 1993
Manifesting carriers of Xp21 muscular dystrophy; lack of correlation between dystrophin expression and clinical weaknessC A Sewry, A Sansome, A Clerk, et al.Neuromuscular Disorders : NMD|June 3, 1998
Early presentation of X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophyF Muntoni, E J Lichtarowicz-Krynska, C A Sewry, et al.Human Molecular Genetics|October 1, 1994
Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletionJ Poulton, K Morten, C Freeman-Emmerson, et al.Human Immunology|May 1, 1988
C4 complement allotypes in juvenile dermatomyositisS A Robb, A H Fielder, C E Saunders, et al.Human Genetics|May 31, 2001
Characterisation of novel point mutations in the survival motor neuron gene SMN, in three patients with SMAL A Skordis, M G Dunckley, L Burglen, et al.Neuromuscular Disorders : NMD|November 2, 1999
Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin statusE Mercuri, J Gruter-Andrew, J Philpot, et al.Human Genetics|April 1, 1997
The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophyI Naom, M D'Alessandro, C Sewry, et al.Plant Biotechnology Journal|March 8, 2016
Production of highly bioactive resveratrol analogues pterostilbene and piceatannol in metabolically engineered grapevine cell culturesAscensión Martínez-Márquez, Jaime A Morante-Carriel, Karla Ramírez-Estrada, et al.Journal of Computer Assisted Tomography|September 1, 1988
Assessment of brain perfusion with MR imagingI R Young, A S Hall, D J Bryant, et al.Pageof 31