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Neurology|August 29, 2001
Diagnosis of Duchenne dystrophy by enhanced detection of small mutationsJ R Mendell, C H Buzin, J Feng, et al.
American Journal of Human Genetics|July 1, 1995
Spectrum of small mutations in the dystrophin coding regionT W Prior, C Bartolo, D K Pearl, et al.
Human Mutation|January 1, 1993
Exon 44 nonsense mutation in two-Duchenne muscular dystrophy brothers detected by heteroduplex analysisT W Prior, A C Papp, P J Snyder, et al.
Neuromuscular Disorders : NMD|March 11, 2017
The 100-meter timed test: Normative data in healthy males and comparative pilot outcome data for use in Duchenne muscular dystrophy clinical trialsLindsay N Alfano, Natalie F Miller, Katherine M Berry, et al.
Nature Genetics|August 1, 1993
A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patientT W Prior, A C Papp, P J Snyder, et al.
Human Immunology|March 1, 1981
Statistical methods for studying homozygous typing cells of unknown specificityN R Mendell, A H Johnson, F E Ward, et al.
Journal of Clinical and Translational Science|April 9, 2025
Development of a job satisfaction measure for clinical research professionals: A mixed methods approachJacqueline M Knapke, John Kues, Spencer K Harris, et al.
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