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Showing results (761-770 of 826) with videos related to

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Human Mutation|July 29, 2022
De novo putative loss-of-function variants in TAF4 are associated with a neuro-developmental disorderBeau D E Janssen, Marie-Jose H van den Boogaard, Klaske Lichtenbelt, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 5, 2001
Treatment with nephrectomy only for small, stage I/favorable histology Wilms' tumor: a report from the National Wilms' Tumor Study GroupD M Green, N E Breslow, J B Beckwith, et al.
International Journal of Molecular Sciences|December 11, 2022
Potential of Non-Coding RNA as Biomarkers for Progressive Supranuclear PalsyFabio A Simoes, Greig Joilin, Oliver Peters, et al.
Nature Genetics|March 12, 2014
Mutations in TJP2 cause progressive cholestatic liver diseaseMelissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, et al.
Addiction (Abingdon, England)|May 31, 2016
Improving the delivery of brief interventions for heavy drinking in primary health care: outcome results of the Optimizing Delivery of Health Care Intervention (ODHIN) five-country cluster randomized factorial trialPeter Anderson, Preben Bendtsen, Fredrik Spak, et al.
Plos Biology|September 14, 2007
High-throughput in vivo analysis of gene expression in Caenorhabditis elegansRebecca Hunt-Newbury, Ryan Viveiros, Robert Johnsen, et al.
Implementation Science : IS|July 17, 2016
Impact of primary healthcare providers' initial role security and therapeutic commitment on implementing brief interventions in managing risky alcohol consumption: a cluster randomised factorial trialM Keurhorst, P Anderson, M Heinen, et al.
American Journal of Medical Genetics. Part A|September 27, 2016
Clinical and genetic aspects of KBG syndromeKaren Low, Tazeen Ashraf, Natalie Canham, et al.
American Journal of Medical Genetics. Part A|July 18, 2019
PAPSS2-related brachyolmia: Clinical and radiological phenotype in 18 new casesLucy Bownass, Stephen Abbs, Ruth Armstrong, et al.
Plos Genetics|March 18, 2015
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairmentPía Villanueva, Ron Nudel, Alexander Hoischen, et al.
Pageof 83

Showing results (761-770 of 826) with videos related to

Sort By:
Pageof 83
Human Mutation|July 29, 2022
De novo putative loss-of-function variants in TAF4 are associated with a neuro-developmental disorderBeau D E Janssen, Marie-Jose H van den Boogaard, Klaske Lichtenbelt, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 5, 2001
Treatment with nephrectomy only for small, stage I/favorable histology Wilms' tumor: a report from the National Wilms' Tumor Study GroupD M Green, N E Breslow, J B Beckwith, et al.
International Journal of Molecular Sciences|December 11, 2022
Potential of Non-Coding RNA as Biomarkers for Progressive Supranuclear PalsyFabio A Simoes, Greig Joilin, Oliver Peters, et al.
Nature Genetics|March 12, 2014
Mutations in TJP2 cause progressive cholestatic liver diseaseMelissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, et al.
Addiction (Abingdon, England)|May 31, 2016
Improving the delivery of brief interventions for heavy drinking in primary health care: outcome results of the Optimizing Delivery of Health Care Intervention (ODHIN) five-country cluster randomized factorial trialPeter Anderson, Preben Bendtsen, Fredrik Spak, et al.
Plos Biology|September 14, 2007
High-throughput in vivo analysis of gene expression in Caenorhabditis elegansRebecca Hunt-Newbury, Ryan Viveiros, Robert Johnsen, et al.
Implementation Science : IS|July 17, 2016
Impact of primary healthcare providers' initial role security and therapeutic commitment on implementing brief interventions in managing risky alcohol consumption: a cluster randomised factorial trialM Keurhorst, P Anderson, M Heinen, et al.
American Journal of Medical Genetics. Part A|September 27, 2016
Clinical and genetic aspects of KBG syndromeKaren Low, Tazeen Ashraf, Natalie Canham, et al.
American Journal of Medical Genetics. Part A|July 18, 2019
PAPSS2-related brachyolmia: Clinical and radiological phenotype in 18 new casesLucy Bownass, Stephen Abbs, Ruth Armstrong, et al.
Plos Genetics|March 18, 2015
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairmentPía Villanueva, Ron Nudel, Alexander Hoischen, et al.
Pageof 83