Showing results (201-210 of 246) with videos related to
Sort By:
Pageof 25
European Journal of Human Genetics : EJHG|January 1, 1996
Prenatal prediction of spinal muscular atrophy. Experience with linkage studies and consequences of present SMN deletion analysisJ M Cobben, H Scheffer, M De Visser, et al.Heredity|July 4, 2018
Unraveling the causes of adaptive benefits of synonymous mutations in TEM-1 β-lactamaseMark P Zwart, Martijn F Schenk, Sungmin Hwang, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
Late onset axonal Charcot-Marie-Tooth phenotype caused by a novel myelin protein zero mutationH M E Bienfait, C G Faber, F Baas, et al.Proceedings. Biological Sciences|March 28, 2009
An experimental test of the independent action hypothesis in virus-insect pathosystemsMark P Zwart, Lia Hemerik, Jenny S Cory, et al.Neuromuscular Disorders : NMD|July 17, 1999
Cardiac involvement in carriers of Duchenne and Becker muscular dystrophyE M Hoogerwaard, P A van der Wouw, A A Wilde, et al.Neuromuscular Disorders : NMD|January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophiesI Richard, N Bourg, S Marchand, et al.Journal of Neurology|June 26, 2008
A natural history study of late onset spinal muscular atrophy types 3b and 4S Piepers, L H van den Berg, F Brugman, et al.Animal Microbiome|August 19, 2022
Succession in the caecal microbiota of developing broilers colonised by extended-spectrum β-lactamase-producing Escherichia coliIngrid Cárdenas-Rey, Teresita D J Bello Gonzalez, Jeanet van der Goot, et al.Neuromuscular Disorders : NMD|October 17, 2003
Comparison of maximal voluntary isometric contraction and hand-held dynamometry in measuring muscle strength of patients with progressive lower motor neuron syndromeJ Visser, E Mans, M de Visser, et al.Neurology|August 28, 2002
Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophyA J van der Kooi, G Bonne, B Eymard, et al.Pageof 25