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Showing results (371-380 of 406) with videos related to

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Journal of Medical Genetics|June 9, 2017
Loss of function in <i>ROBO1</i> is associated with tetralogy of Fallot and septal defectsPaul Kruszka, Pranoot Tanpaiboon, Katherine Neas, et al.
Nature Communications|October 7, 2023
Immediate neural impact and incomplete compensation after semantic hub disconnectionZsuzsanna Kocsis, Rick L Jenison, Peter N Taylor, et al.
Molecular Psychiatry|September 23, 2018
Stress-inducible-stem cells: a new view on endocrine, metabolic and mental disease?S R Bornstein, C Steenblock, G P Chrousos, et al.
American Journal of Human Genetics|January 25, 2025
Advancing long-read nanopore genome assembly and accurate variant calling for rare disease detectionShloka Negi, Sarah L Stenton, Seth I Berger, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Genome sequencing reveals the impact of non-canonical exon inclusions in rare genetic diseaseGeorgia Pitsava, Megan Hawley, Light Auriga, et al.
Journal of Molecular Biology|April 28, 2016
The Nucleosome Remodeling and Deacetylase Complex NuRD Is Built from Preformed Catalytically Active Sub-modulesW Zhang, A Aubert, J M Gomez de Segura, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 10, 2025
Genome sequencing reveals the impact of pseudoexons in rare genetic diseaseGeorgia Pitsava, Megan Hawley, Light Auriga, et al.
The European Respiratory Journal|November 28, 2019
Technical standards for respiratory oscillometryGregory G King, Jason Bates, Kenneth I Berger, et al.
European Respiratory Review : an Official Journal of the European Respiratory Society|February 10, 2022
Clinical significance and applications of oscillometryDavid A Kaminsky, Shannon J Simpson, Kenneth I Berger, et al.
Arxiv|January 30, 2023
Beyond the exome: what's next in diagnostic testing for Mendelian conditionsMonica H Wojcik, Chloe M Reuter, Shruti Marwaha, et al.
Pageof 41

Showing results (371-380 of 406) with videos related to

Sort By:
Pageof 41
Journal of Medical Genetics|June 9, 2017
Loss of function in <i>ROBO1</i> is associated with tetralogy of Fallot and septal defectsPaul Kruszka, Pranoot Tanpaiboon, Katherine Neas, et al.
Nature Communications|October 7, 2023
Immediate neural impact and incomplete compensation after semantic hub disconnectionZsuzsanna Kocsis, Rick L Jenison, Peter N Taylor, et al.
Molecular Psychiatry|September 23, 2018
Stress-inducible-stem cells: a new view on endocrine, metabolic and mental disease?S R Bornstein, C Steenblock, G P Chrousos, et al.
American Journal of Human Genetics|January 25, 2025
Advancing long-read nanopore genome assembly and accurate variant calling for rare disease detectionShloka Negi, Sarah L Stenton, Seth I Berger, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Genome sequencing reveals the impact of non-canonical exon inclusions in rare genetic diseaseGeorgia Pitsava, Megan Hawley, Light Auriga, et al.
Journal of Molecular Biology|April 28, 2016
The Nucleosome Remodeling and Deacetylase Complex NuRD Is Built from Preformed Catalytically Active Sub-modulesW Zhang, A Aubert, J M Gomez de Segura, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 10, 2025
Genome sequencing reveals the impact of pseudoexons in rare genetic diseaseGeorgia Pitsava, Megan Hawley, Light Auriga, et al.
The European Respiratory Journal|November 28, 2019
Technical standards for respiratory oscillometryGregory G King, Jason Bates, Kenneth I Berger, et al.
European Respiratory Review : an Official Journal of the European Respiratory Society|February 10, 2022
Clinical significance and applications of oscillometryDavid A Kaminsky, Shannon J Simpson, Kenneth I Berger, et al.
Arxiv|January 30, 2023
Beyond the exome: what's next in diagnostic testing for Mendelian conditionsMonica H Wojcik, Chloe M Reuter, Shruti Marwaha, et al.
Pageof 41