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V Morgan

Showing results (141-150 of 278) with videos related to

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Pediatric Pulmonology|March 21, 2012
Interpretation of pediatric lung function: impact of ethnicityJ Kirkby, R Bonner, S Lum, et al.
Circulation. Cardiovascular Imaging|July 7, 2011
Diagnostic value of vena contracta area in the quantification of mitral regurgitation severity by color Doppler 3D echocardiographyXin Zeng, Robert A Levine, Lanqi Hua, et al.
Molecular Psychiatry|May 25, 2007
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophreniaT Lencz, T V Morgan, M Athanasiou, et al.
Journal of Clinical Medicine|October 29, 2020
Cell-Free DNA in the Investigation of MiscarriageEmily Colley, Adam J Devall, Helen Williams, et al.
Platelets|March 8, 2017
Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet functionAnnabel Maclachlan, Gerry Dolan, Charlotte Grimley, et al.
Annals of Surgical Oncology|May 20, 2024
Impact of Neoadjuvant Chemoimmunotherapy on Surgical Outcomes and Time to Radiation in Triple-Negative Breast CancerSara P Myers, Varadan Sevilimedu, V Morgan Jones, et al.
The Australian and New Zealand Journal of Psychiatry|May 2, 2000
Psychotic disorders in urban areas: an overview of the Study on Low Prevalence DisordersA Jablensky, J McGrath, H Herrman, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 2020
Asteroid impact, not volcanism, caused the end-Cretaceous dinosaur extinctionAlfio Alessandro Chiarenza, Alexander Farnsworth, Philip D Mannion, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 16, 2026
Performing Large-Scale Genetic Analysis in the Bleeding Disorders CommunityAnna R Blankstein, Sterre P E Willems, Saskia E M Schols, et al.
The Turkish Journal of Pediatrics|June 2, 2009
Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 geneHakan Cangül, Ozlem Ozdemir, Tahsin Yakut, et al.
Pageof 28

Showing results (141-150 of 278) with videos related to

Sort By:
Pageof 28
Pediatric Pulmonology|March 21, 2012
Interpretation of pediatric lung function: impact of ethnicityJ Kirkby, R Bonner, S Lum, et al.
Circulation. Cardiovascular Imaging|July 7, 2011
Diagnostic value of vena contracta area in the quantification of mitral regurgitation severity by color Doppler 3D echocardiographyXin Zeng, Robert A Levine, Lanqi Hua, et al.
Molecular Psychiatry|May 25, 2007
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophreniaT Lencz, T V Morgan, M Athanasiou, et al.
Journal of Clinical Medicine|October 29, 2020
Cell-Free DNA in the Investigation of MiscarriageEmily Colley, Adam J Devall, Helen Williams, et al.
Platelets|March 8, 2017
Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet functionAnnabel Maclachlan, Gerry Dolan, Charlotte Grimley, et al.
Annals of Surgical Oncology|May 20, 2024
Impact of Neoadjuvant Chemoimmunotherapy on Surgical Outcomes and Time to Radiation in Triple-Negative Breast CancerSara P Myers, Varadan Sevilimedu, V Morgan Jones, et al.
The Australian and New Zealand Journal of Psychiatry|May 2, 2000
Psychotic disorders in urban areas: an overview of the Study on Low Prevalence DisordersA Jablensky, J McGrath, H Herrman, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 2020
Asteroid impact, not volcanism, caused the end-Cretaceous dinosaur extinctionAlfio Alessandro Chiarenza, Alexander Farnsworth, Philip D Mannion, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 16, 2026
Performing Large-Scale Genetic Analysis in the Bleeding Disorders CommunityAnna R Blankstein, Sterre P E Willems, Saskia E M Schols, et al.
The Turkish Journal of Pediatrics|June 2, 2009
Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 geneHakan Cangül, Ozlem Ozdemir, Tahsin Yakut, et al.
Pageof 28