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Pediatrics|August 18, 2017
Public Health Literature Review of Fragile X SyndromeMelissa Raspa, Anne C Wheeler, Catharine RileyPublic Health Genomics|April 15, 2025
Informational, Support, and Educational Needs of Parents of Children with Sickle Cell TraitMolly Lynch, Rebecca Wright, Melissa Raspa, et al.Frontiers in Pediatrics|March 10, 2022
Severe Combined Immunodeficiency: Knowledge and Information Needs Among Healthcare ProvidersOksana Kutsa, Angela Gwaltney, Alissa Creamer, et al.American Journal on Intellectual and Developmental Disabilities|October 16, 2010
Using a parent survey to advance knowledge about the nature and consequences of fragile X syndromeDonald B Bailey, Melissa Raspa, Murrey G OlmstedInteractive Journal of Medical Research|February 25, 2021
Barriers and Facilitators to Genetic Service Delivery Models: Scoping ReviewMelissa Raspa, Rebecca Moultrie, Danielle Toth, et al.American Journal on Intellectual and Developmental Disabilities|January 24, 2014
Modeling family adaptation to fragile X syndromeMelissa Raspa, Donald B Bailey, Carla Bann, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2012
Caregiver opinions about fragile X population screeningDonald B Bailey, Ellen Bishop, Melissa Raspa, et al.Frontiers in Public Health|February 27, 2026
An evaluation of U.S. federal investments in newborn screening: successes, gaps, and future directionsMelissa Raspa, Rebecca Wright, Sara M Andrews, et al.Pediatrics|July 8, 2009
No change in the age of diagnosis for fragile x syndrome: findings from a national parent surveyDonald B Bailey, Melissa Raspa, Ellen Bishop, et al.American Journal of Medical Genetics. Part A|June 24, 2008
Co-occurring conditions associated with FMR1 gene variations: findings from a national parent surveyDonald B Bailey, Melissa Raspa, Murrey Olmsted, et al.Pageof 7