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Journal of Genetic Counseling|March 3, 2019
Clinical models of telehealth in genetics: A regional telegenetics landscapeAlissa B Terry, Amanda Wylie, Melissa Raspa, et al.American Journal on Intellectual and Developmental Disabilities|February 5, 2019
A Description of the Educational Setting Among Individuals With Fragile X SyndromeRebecca Nash, Catharine Riley, Pangaja Paramsothy, et al.JAMA Network Open|December 29, 2021
Expert Evaluation of Strategies to Modernize Newborn Screening in the United StatesDonald B Bailey, Katherine Ackerman Porter, Sara M Andrews, et al.Journal of Autism and Developmental Disorders|July 1, 2015
Autism Symptoms Across Adulthood in Men with Fragile X Syndrome: A Cross-Sectional AnalysisSigan L Hartley, Anne C Wheeler, Marsha R Mailick, et al.Brain Sciences|January 6, 2019
Early Identification of Fragile X Syndrome through Expanded Newborn ScreeningKatherine C Okoniewski, Anne C Wheeler, Stacey Lee, et al.Journal of Empirical Research on Human Research Ethics : JERHRE|November 26, 2014
Parent ratings of ability to consent for clinical trials in fragile X syndromeDonald B Bailey, Melissa Raspa, Anne Wheeler, et al.Journal of Medical Internet Research|May 22, 2020
Ethical, Legal, and Social Issues Related to the Inclusion of Individuals With Intellectual Disabilities in Electronic Health Record Research: Scoping ReviewMelissa Raspa, Rebecca Moultrie, Laura Wagner, et al.Journal of Autism and Developmental Disorders|November 28, 2022
Latent Class Analysis Identifies Distinctive Behavioral Subtypes in Children with Fragile X SyndromeWalter E Kaufmann, Melissa Raspa, Carla M Bann, et al.Frontiers in Immunology|May 22, 2020
Information and Emotional Support Needs of Families Whose Infant Was Diagnosed With SCID Through Newborn ScreeningMelissa Raspa, Molly Lynch, Linda Squiers, et al.Orphanet Journal of Rare Diseases|October 28, 2022
Parental coping with uncertainties along the severe combined immunodeficiency journeyOksana Kutsa, Sara M Andrews, Erin Mallonee, et al.Pageof 7