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Jonathan S Berg

Showing results (91-100 of 168) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 25, 2020
An approach to integrating exome sequencing for fetal structural anomalies into clinical practiceNeeta L Vora, Kelly Gilmore, Alicia Brandt, et al.
American Journal of Human Genetics|July 4, 2015
Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and AdolescentsJeffrey R Botkin, John W Belmont, Jonathan S Berg, et al.
The Journal of Experimental Medicine|August 18, 2018
h<i>CALCRL</i> mutation causes autosomal recessive nonimmune hydrops fetalis with lymphatic dysplasiaDuncan I Mackie, Fuad Al Mutairi, Reema B Davis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2013
Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologiesKatrina A B Goddard, Evelyn P Whitlock, Jonathan S Berg, et al.
Trials|June 29, 2018
Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocolLaura V Milko, Christine Rini, Megan A Lewis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
The who, what, and why of research participants' intentions to request a broad range of secondary findings in a diagnostic genomic sequencing studyChristine Rini, Cynthia M Khan, Elizabeth Moore, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 22, 2018
Factors influencing NCGENES research participants' requests for non-medically actionable secondary findingsMyra I Roche, Ida Griesemer, Cynthia M Khan, et al.
Physical & Occupational Therapy in Pediatrics|October 31, 2022
The Burden of COVID-19 on Caregivers of Children with Suspected Genetic Conditions: A Therapeutic OdysseyMargaret Waltz, Courtney Canter, Jeannette T Bensen, et al.
NPJ Genomic Medicine|December 17, 2019
FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulationLaura V Milko, Flavia Chen, Kee Chan, et al.
Human Molecular Genetics|July 4, 2019
Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathyMadhurima Saha, Skylar A Rizzo, Manashwi Ramanathan, et al.
Pageof 17

Showing results (91-100 of 168) with videos related to

Sort By:
Pageof 17
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 25, 2020
An approach to integrating exome sequencing for fetal structural anomalies into clinical practiceNeeta L Vora, Kelly Gilmore, Alicia Brandt, et al.
American Journal of Human Genetics|July 4, 2015
Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and AdolescentsJeffrey R Botkin, John W Belmont, Jonathan S Berg, et al.
The Journal of Experimental Medicine|August 18, 2018
h<i>CALCRL</i> mutation causes autosomal recessive nonimmune hydrops fetalis with lymphatic dysplasiaDuncan I Mackie, Fuad Al Mutairi, Reema B Davis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2013
Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologiesKatrina A B Goddard, Evelyn P Whitlock, Jonathan S Berg, et al.
Trials|June 29, 2018
Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocolLaura V Milko, Christine Rini, Megan A Lewis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
The who, what, and why of research participants' intentions to request a broad range of secondary findings in a diagnostic genomic sequencing studyChristine Rini, Cynthia M Khan, Elizabeth Moore, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 22, 2018
Factors influencing NCGENES research participants' requests for non-medically actionable secondary findingsMyra I Roche, Ida Griesemer, Cynthia M Khan, et al.
Physical & Occupational Therapy in Pediatrics|October 31, 2022
The Burden of COVID-19 on Caregivers of Children with Suspected Genetic Conditions: A Therapeutic OdysseyMargaret Waltz, Courtney Canter, Jeannette T Bensen, et al.
NPJ Genomic Medicine|December 17, 2019
FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulationLaura V Milko, Flavia Chen, Kee Chan, et al.
Human Molecular Genetics|July 4, 2019
Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathyMadhurima Saha, Skylar A Rizzo, Manashwi Ramanathan, et al.
Pageof 17