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Showing results (291-300 of 566) with videos related to

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Nature|July 5, 1987
A cDNA clone from the Duchenne/Becker muscular dystrophy geneA H Burghes, C Logan, X Hu, et al.
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|May 31, 2022
Patient and Family Factors Associated with Use of Telemedicine Visits for Pediatric Acute Respiratory Tract Infections, 2018-2019Samuel R Wittman, Jonathan G Yabes, Lindsay M Sabik, et al.
Journal of Visualized Experiments : Jove|June 13, 2017
Laboratory Techniques Used to Maintain and Differentiate Biotypes of Vibrio cholerae Clinical and Environmental IsolatesKyle D Brumfield, Bailey M Carignan, Jordan N Ray, et al.
Muscle & Nerve|April 14, 2012
Milder phenotype of congenital muscular dystrophy in a novel POMT1 mutationSamiah A Al-Zaidy, Berivan Baskin, Cynthia Hawkins, et al.
Human Molecular Genetics|May 1, 1993
Genomic organization of exons 22 to 25 of the dystrophin geneK G Bebchuk, D E Bulman, V N D'Souza, et al.
Genomics|June 1, 1991
Point mutation in the human dystrophin gene: identification through western blot analysisD E Bulman, S B Gangopadhyay, K G Bebchuck, et al.
Comprehensive Psychiatry|November 20, 2013
Suicide attempts before joining the military increase risk for suicide attempts and severity of suicidal ideation among military personnel and veteransCraig J Bryan, AnnaBelle O Bryan, Bobbie N Ray-Sannerud, et al.
Indian Journal of Pediatrics|April 25, 2000
Changes in anti-oxidant enzymes and lipid peroxidation in hyaline membrane diseaseS K Singh, A Tandon, S Kumari, et al.
BMJ Quality & Safety|November 28, 2017
Transportation characteristics associated with non-arrivals to paediatric clinic appointments: a retrospective analysis of 51 580 scheduled visitsDavid J Wallace, Kristin N Ray, Abbye Degan, et al.
Journal of Medical Genetics|June 27, 2001
A missense mutation in the SEDL gene results in delayed onset of X linked spondyloepiphyseal dysplasia in a large pedigreeE Grunebaum, E Arpaia, J J MacKenzie, et al.
Pageof 57

Showing results (291-300 of 566) with videos related to

Sort By:
Pageof 57
Nature|July 5, 1987
A cDNA clone from the Duchenne/Becker muscular dystrophy geneA H Burghes, C Logan, X Hu, et al.
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|May 31, 2022
Patient and Family Factors Associated with Use of Telemedicine Visits for Pediatric Acute Respiratory Tract Infections, 2018-2019Samuel R Wittman, Jonathan G Yabes, Lindsay M Sabik, et al.
Journal of Visualized Experiments : Jove|June 13, 2017
Laboratory Techniques Used to Maintain and Differentiate Biotypes of Vibrio cholerae Clinical and Environmental IsolatesKyle D Brumfield, Bailey M Carignan, Jordan N Ray, et al.
Muscle & Nerve|April 14, 2012
Milder phenotype of congenital muscular dystrophy in a novel POMT1 mutationSamiah A Al-Zaidy, Berivan Baskin, Cynthia Hawkins, et al.
Human Molecular Genetics|May 1, 1993
Genomic organization of exons 22 to 25 of the dystrophin geneK G Bebchuk, D E Bulman, V N D'Souza, et al.
Genomics|June 1, 1991
Point mutation in the human dystrophin gene: identification through western blot analysisD E Bulman, S B Gangopadhyay, K G Bebchuck, et al.
Comprehensive Psychiatry|November 20, 2013
Suicide attempts before joining the military increase risk for suicide attempts and severity of suicidal ideation among military personnel and veteransCraig J Bryan, AnnaBelle O Bryan, Bobbie N Ray-Sannerud, et al.
Indian Journal of Pediatrics|April 25, 2000
Changes in anti-oxidant enzymes and lipid peroxidation in hyaline membrane diseaseS K Singh, A Tandon, S Kumari, et al.
BMJ Quality & Safety|November 28, 2017
Transportation characteristics associated with non-arrivals to paediatric clinic appointments: a retrospective analysis of 51 580 scheduled visitsDavid J Wallace, Kristin N Ray, Abbye Degan, et al.
Journal of Medical Genetics|June 27, 2001
A missense mutation in the SEDL gene results in delayed onset of X linked spondyloepiphyseal dysplasia in a large pedigreeE Grunebaum, E Arpaia, J J MacKenzie, et al.
Pageof 57