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Cynthia M Powell

Showing results (41-50 of 65) with videos related to

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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.
Clinical and Translational Science|December 31, 2020
Outreach to new mothers through direct mail and email: recruitment in the Early Check research studyRyan S Paquin, Megan A Lewis, Blake A Harper, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2016
Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and GenomicsFrederick R Bieber, Athena M Cherry, Beverly S Emanuel, et al.
JAMA Network Open|February 1, 2020
Evaluation of X-Linked Adrenoleukodystrophy Newborn Screening in North CarolinaStacey Lee, Kristin Clinard, Sarah P Young, et al.
The Journal of Pediatrics|May 29, 2019
The North Carolina Experience with Mucopolysaccharidosis Type I Newborn ScreeningJennifer L Taylor, Kristin Clinard, Cynthia M Powell, et al.
JAMA Pediatrics|February 15, 2021
Novel Variant Findings and Challenges Associated With the Clinical Integration of Genomic Testing: An Interim Report of the Genomic Medicine for Ill Neonates and Infants (GEMINI) StudyJill L Maron, Stephen F Kingsmore, Kristen Wigby, et al.
JAMA|July 11, 2023
Rapid Whole-Genomic Sequencing and a Targeted Neonatal Gene Panel in Infants With a Suspected Genetic DisorderJill L Maron, Stephen Kingsmore, Bruce D Gelb, et al.
International Journal of Neonatal Screening|April 3, 2021
A Voluntary Statewide Newborn Screening Pilot for Spinal Muscular Atrophy: Results from Early CheckKaterina S Kucera, Jennifer L Taylor, Veronica R Robles, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2017
Prenatal exome sequencing in anomalous fetuses: new opportunities and challengesNeeta L Vora, Bradford Powell, Alicia Brandt, et al.
Nature Communications|June 6, 2013
Stac3 is a component of the excitation-contraction coupling machinery and mutated in Native American myopathyEric J Horstick, Jeremy W Linsley, James J Dowling, et al.
Pageof 7

Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
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.
Clinical and Translational Science|December 31, 2020
Outreach to new mothers through direct mail and email: recruitment in the Early Check research studyRyan S Paquin, Megan A Lewis, Blake A Harper, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2016
Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and GenomicsFrederick R Bieber, Athena M Cherry, Beverly S Emanuel, et al.
JAMA Network Open|February 1, 2020
Evaluation of X-Linked Adrenoleukodystrophy Newborn Screening in North CarolinaStacey Lee, Kristin Clinard, Sarah P Young, et al.
The Journal of Pediatrics|May 29, 2019
The North Carolina Experience with Mucopolysaccharidosis Type I Newborn ScreeningJennifer L Taylor, Kristin Clinard, Cynthia M Powell, et al.
JAMA Pediatrics|February 15, 2021
Novel Variant Findings and Challenges Associated With the Clinical Integration of Genomic Testing: An Interim Report of the Genomic Medicine for Ill Neonates and Infants (GEMINI) StudyJill L Maron, Stephen F Kingsmore, Kristen Wigby, et al.
JAMA|July 11, 2023
Rapid Whole-Genomic Sequencing and a Targeted Neonatal Gene Panel in Infants With a Suspected Genetic DisorderJill L Maron, Stephen Kingsmore, Bruce D Gelb, et al.
International Journal of Neonatal Screening|April 3, 2021
A Voluntary Statewide Newborn Screening Pilot for Spinal Muscular Atrophy: Results from Early CheckKaterina S Kucera, Jennifer L Taylor, Veronica R Robles, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2017
Prenatal exome sequencing in anomalous fetuses: new opportunities and challengesNeeta L Vora, Bradford Powell, Alicia Brandt, et al.
Nature Communications|June 6, 2013
Stac3 is a component of the excitation-contraction coupling machinery and mutated in Native American myopathyEric J Horstick, Jeremy W Linsley, James J Dowling, et al.
Pageof 7