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American Journal of Public Health|October 1, 2005
Newborn screening for developmental disabilities: reframing presumptive benefitDonald B Bailey, Debra Skinner, Steven F WarrenJournal of Pediatric Psychology|April 2, 2008
Supporting family adaptation to presymptomatic and "untreatable" conditions in an era of expanded newborn screeningDonald B Bailey, F Daniel Armstrong, Alex R Kemper, et al.Pediatrics|February 4, 2003
Discovering fragile X syndrome: family experiences and perceptionsDonald B Bailey, Debra Skinner, Karen L SparkmanGenetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2003
Screening for Fragile X Syndrome: parent attitudes and perspectivesDebra Skinner, Karen L Sparkman, Donald B BaileyGenetics 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.Social Science & Medicine (1982)|June 15, 2007
A place for genetic uncertainty: parents valuing an unknown in the meaning of diseaseIan Whitmarsh, Arlene M Davis, Debra Skinner, et al.Mental Retardation and Developmental Disabilities Research Reviews|December 22, 2006
Changing perspectives on the benefits of newborn screeningDonald B Bailey, Laura M Beskow, Arlene M Davis, et al.Pediatrics|March 4, 2008
Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issuesDonald B Bailey, Debra Skinner, Arlene M Davis, et al.American Journal on Intellectual and Developmental Disabilities|June 22, 2012
Parenting young children with and without Fragile X syndromeAudra Sterling, Leah Barnum, Debra Skinner, et al.Pediatrics|June 1, 2011
Parents' decisions to screen newborns for FMR1 gene expansions in a pilot research projectDebra Skinner, Summer Choudhury, John Sideris, et al.Pageof 18