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Angus Clarke

Showing results (91-100 of 111) with videos related to

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Human Reproduction Open|September 7, 2019
Human germline gene editing. Recommendations of ESHG and ESHREGuido de Wert, Guido Pennings, Angus Clarke, et al.
European Journal of Human Genetics : EJHG|January 13, 2018
Responsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHREGuido De Wert, Björn Heindryckx, Guido Pennings, et al.
Human Reproduction Open|September 7, 2019
Responsible innovation in human germline gene editing. Background document to the recommendations of ESHG and ESHREGuido de Wert, Björn Heindryckx, Guido Pennings, et al.
NIHR Open Research|October 25, 2023
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocolCeline Lewis, James Buchanan, Angus Clarke, et al.
European Journal of Human Genetics : EJHG|December 14, 2025
Cascade counselling and testing. Recommendations of the European Society of Human GeneticsGuido de Wert, Carla G van El, Angus Clarke, et al.
American Journal of Human Genetics|October 20, 2004
Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardationLinda S Weaving, John Christodoulou, Sarah L Williamson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 14, 2018
Including ELSI research questions in newborn screening pilot studiesAaron J Goldenberg, Michele Lloyd-Puryear, Jeffrey P Brosco, et al.
European Journal of Human Genetics : EJHG|November 23, 2020
Opportunistic genomic screening. Recommendations of the European Society of Human GeneticsGuido de Wert, Wybo Dondorp, Angus Clarke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2018
27 years of prenatal diagnosis for Huntington disease in the United KingdomRaul E Piña-Aguilar, Sheila A Simpson, Abdulrahman Alshatti, et al.
American Journal of Human Genetics|January 28, 2014
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defectsKathleen A Williamson, Joe Rainger, James A B Floyd, et al.
Pageof 12

Showing results (91-100 of 111) with videos related to

Sort By:
Pageof 12
Human Reproduction Open|September 7, 2019
Human germline gene editing. Recommendations of ESHG and ESHREGuido de Wert, Guido Pennings, Angus Clarke, et al.
European Journal of Human Genetics : EJHG|January 13, 2018
Responsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHREGuido De Wert, Björn Heindryckx, Guido Pennings, et al.
Human Reproduction Open|September 7, 2019
Responsible innovation in human germline gene editing. Background document to the recommendations of ESHG and ESHREGuido de Wert, Björn Heindryckx, Guido Pennings, et al.
NIHR Open Research|October 25, 2023
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocolCeline Lewis, James Buchanan, Angus Clarke, et al.
European Journal of Human Genetics : EJHG|December 14, 2025
Cascade counselling and testing. Recommendations of the European Society of Human GeneticsGuido de Wert, Carla G van El, Angus Clarke, et al.
American Journal of Human Genetics|October 20, 2004
Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardationLinda S Weaving, John Christodoulou, Sarah L Williamson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 14, 2018
Including ELSI research questions in newborn screening pilot studiesAaron J Goldenberg, Michele Lloyd-Puryear, Jeffrey P Brosco, et al.
European Journal of Human Genetics : EJHG|November 23, 2020
Opportunistic genomic screening. Recommendations of the European Society of Human GeneticsGuido de Wert, Wybo Dondorp, Angus Clarke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2018
27 years of prenatal diagnosis for Huntington disease in the United KingdomRaul E Piña-Aguilar, Sheila A Simpson, Abdulrahman Alshatti, et al.
American Journal of Human Genetics|January 28, 2014
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defectsKathleen A Williamson, Joe Rainger, James A B Floyd, et al.
Pageof 12