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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.
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.
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