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Showing results (471-480 of 477) with videos related to

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Leukemia|June 11, 2016
Genomic disruption of the histone methyltransferase SETD2 in chronic lymphocytic leukaemiaH Parker, M J J Rose-Zerilli, M Larrayoz, et al.
American Journal of Human Genetics|June 19, 2026
De novo variants in LDB1 are linked to distinct neurodevelopmental phenotypes determined by variant location and differing pathomechanismsRebecca Fluri, Mireia Coll-Tané, Theresa Brunet, et al.
BMJ Global Health|June 8, 2017
Global Surgery 2030: a roadmap for high income country actorsJoshua S Ng-Kamstra, Sarah L M Greenberg, Fizan Abdullah, et al.
American Journal of Human Genetics|December 30, 2025
De novo variants in KDM2A cause a syndromic neurodevelopmental disorderEric N Anderson, Stephan Drukewitz, Sukhleen Kour, et al.
Medrxiv : the Preprint Server for Health Sciences|April 16, 2025
De novo variants in <i>KDM2A</i> cause a syndromic neurodevelopmental disorderEric N Anderson, Stephan Drukewitz, Sukhleen Kour, et al.
Age and Ageing|September 30, 2022
World guidelines for falls prevention and management for older adults: a global initiativeManuel Montero-Odasso, Nathalie van der Velde, Finbarr C Martin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2025
Pathogenic XPO1 variants cause a dominant neurodevelopmental disorderAmber S E van Oirsouw, Pavla Nedbalova, Miroslava Hancarova, et al.
Pageof 48

Showing results (471-480 of 477) with videos related to

Sort By:
Pageof 48
You have reached the last page of results.This site can display upto 477 results.
Leukemia|June 11, 2016
Genomic disruption of the histone methyltransferase SETD2 in chronic lymphocytic leukaemiaH Parker, M J J Rose-Zerilli, M Larrayoz, et al.
American Journal of Human Genetics|June 19, 2026
De novo variants in LDB1 are linked to distinct neurodevelopmental phenotypes determined by variant location and differing pathomechanismsRebecca Fluri, Mireia Coll-Tané, Theresa Brunet, et al.
BMJ Global Health|June 8, 2017
Global Surgery 2030: a roadmap for high income country actorsJoshua S Ng-Kamstra, Sarah L M Greenberg, Fizan Abdullah, et al.
American Journal of Human Genetics|December 30, 2025
De novo variants in KDM2A cause a syndromic neurodevelopmental disorderEric N Anderson, Stephan Drukewitz, Sukhleen Kour, et al.
Medrxiv : the Preprint Server for Health Sciences|April 16, 2025
De novo variants in <i>KDM2A</i> cause a syndromic neurodevelopmental disorderEric N Anderson, Stephan Drukewitz, Sukhleen Kour, et al.
Age and Ageing|September 30, 2022
World guidelines for falls prevention and management for older adults: a global initiativeManuel Montero-Odasso, Nathalie van der Velde, Finbarr C Martin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2025
Pathogenic XPO1 variants cause a dominant neurodevelopmental disorderAmber S E van Oirsouw, Pavla Nedbalova, Miroslava Hancarova, et al.
Pageof 48