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Donald B Bailey

Showing results (91-100 of 109) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2017
Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete-choice experimentMegan A Lewis, Alex Stine, Ryan S Paquin, et al.
Journal of Genetic Counseling|June 28, 2012
Design and evaluation of a decision aid for inviting parents to participate in a fragile X newborn screening pilot studyDonald B Bailey, Megan A Lewis, Shelly L Harris, et al.
Social Science & Medicine (1982)|November 19, 2018
A behavior-theoretic evaluation of values clarification on parental beliefs and intentions toward genomic sequencing for newbornsRyan S Paquin, Susana Peinado, Megan A Lewis, et al.
Plos One|July 27, 2018
Skills attained by infants with congenital Zika syndrome: Pilot data from BrazilAnne C Wheeler, Camila V Ventura, Ty Ridenour, et al.
Nature Reviews. Disease Primers|September 30, 2017
Fragile X syndromeRandi J Hagerman, Elizabeth Berry-Kravis, Heather Cody Hazlett, et al.
Journal of Pediatric Psychology|December 17, 2008
Trajectories and predictors of the development of very young boys with fragile X syndromeJane E Roberts, Jean B Mankowski, John Sideris, et al.
JAMA Network Open|May 6, 2020
Developmental Outcomes Among Young Children With Congenital Zika Syndrome in BrazilAnne C Wheeler, Danielle Toth, Ty Ridenour, et al.
Journal of Neurodevelopmental Disorders|August 7, 2014
Associated features in females with an FMR1 premutationAnne C Wheeler, Donald B Bailey, Elizabeth Berry-Kravis, 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.
Pediatrics|April 29, 2021
Emergence of Developmental Delay in Infants and Toddlers With an <i>FMR1</i> MutationAnne C Wheeler, Angela Gwaltney, Melissa Raspa, et al.
Pageof 11

Showing results (91-100 of 109) with videos related to

Sort By:
Pageof 11
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2017
Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete-choice experimentMegan A Lewis, Alex Stine, Ryan S Paquin, et al.
Journal of Genetic Counseling|June 28, 2012
Design and evaluation of a decision aid for inviting parents to participate in a fragile X newborn screening pilot studyDonald B Bailey, Megan A Lewis, Shelly L Harris, et al.
Social Science & Medicine (1982)|November 19, 2018
A behavior-theoretic evaluation of values clarification on parental beliefs and intentions toward genomic sequencing for newbornsRyan S Paquin, Susana Peinado, Megan A Lewis, et al.
Plos One|July 27, 2018
Skills attained by infants with congenital Zika syndrome: Pilot data from BrazilAnne C Wheeler, Camila V Ventura, Ty Ridenour, et al.
Nature Reviews. Disease Primers|September 30, 2017
Fragile X syndromeRandi J Hagerman, Elizabeth Berry-Kravis, Heather Cody Hazlett, et al.
Journal of Pediatric Psychology|December 17, 2008
Trajectories and predictors of the development of very young boys with fragile X syndromeJane E Roberts, Jean B Mankowski, John Sideris, et al.
JAMA Network Open|May 6, 2020
Developmental Outcomes Among Young Children With Congenital Zika Syndrome in BrazilAnne C Wheeler, Danielle Toth, Ty Ridenour, et al.
Journal of Neurodevelopmental Disorders|August 7, 2014
Associated features in females with an FMR1 premutationAnne C Wheeler, Donald B Bailey, Elizabeth Berry-Kravis, 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.
Pediatrics|April 29, 2021
Emergence of Developmental Delay in Infants and Toddlers With an <i>FMR1</i> MutationAnne C Wheeler, Angela Gwaltney, Melissa Raspa, et al.
Pageof 11